Total (210) | D1 (1) | D2 (25) | D3 (60) | D4 (124) | |
---|---|---|---|---|---|
Premier | 13 (6.19 %) | 13 (10.48 %) | |||
Deuxième | 18 (8.57 %) | 4 (6.67 %) | 14 (11.29 %) | ||
Troisième | 16 (7.62 %) | 1 (1.67 %) | 15 (12.10 %) |
Eq | Saison | Div | Tour | Match | Neg | Plc | IC | ADV |
---|---|---|---|---|---|---|---|---|
STA | 2017 | 3 | 9 | LRVa(43.0)-STA(35.0) | -213 | 10 | 3.0 | 5.0 |
STA | 2017 | 3 | 8 | VRAa(39.0)-STA(39.0) | -276 | 8 | 5.0 | 4.0 |
STA | 2017 | 3 | 7 | STA(39.0)-BOU(39.0) | -155 | 8 | 5.0 | 4.0 |
STA | 2017 | 3 | 6 | STA(48.5)-ACJb(29.5) | -133 | 5 | 8.0 | 1.0 |
STA | 2017 | 3 | 3 | STA(37.0)-LRVa(41.0) | -137 | 8 | 5.0 | 4.0 |
STA | 2017 | 3 | 2 | STA(52.0)-VRAa(26.0) | -216 | 10 | 3.0 | 4.0 |
STA | 2017 | 3 | 1 | BOU(46.0)-STA(32.0) | -266 | 11 | 2.0 | 5.0 |
STA | 2016 | 3 | 11 | STA(34.5)-PHEa(43.5) | -343 | 12 | 1.0 | 6.0 |
STA | 2016 | 3 | 10 | STA(31.0)-SABc(47.0) | -198 | 8 | 5.0 | 4.0 |
STA | 2016 | 3 | 8 | STA(39.0)-ACJb(39.0) | -269 | 10 | 3.0 | 5.0 |
STA | 2016 | 3 | 6 | PHEa(36.0)-STA(42.0) | -225 | 12 | 1.0 | 6.0 |
STA | 2016 | 3 | 4 | SABc(42.0)-STA(36.0) | -115 | 10 | 3.0 | 6.0 |
STA | 2016 | 3 | 1 | STA(38.0)-RECa(40.0) | -236 | 8 | 5.0 | 4.0 |
STA | 2014 | 4 | 10 | KAKb(16.0)-STA(39.0) | -198 | 4 | 7.0 | 0.0 |
STA | 2014 | 4 | 9 | PHEb(20.0)-STA(35.0) | -129 | 5 | 6.0 | 1.0 |
STA | 2014 | 4 | 8 | STA(27.0)-KIH(28.0) | -196 | 9 | 2.0 | 5.0 |
STA | 2014 | 4 | 7 | STA(23.0)-RECa(32.0) | -136 | 7 | 4.0 | 4.0 |
STA | 2014 | 4 | 6 | SABc(19.0)-STA(36.0) | -139 | 3 | 8.0 | 0.0 |
STA | 2014 | 4 | 5 | STA(39.0)-KAKb(16.0) | -131 | 3 | 8.0 | 0.0 |
STA | 2014 | 4 | 4 | STA(35.0)-PHEb(20.0) | -34 | 3 | 8.0 | 0.0 |
STA | 2014 | 4 | 3 | KIH(24.0)-STA(31.0) | -135 | 7 | 4.0 | 3.0 |
STA | 2014 | 4 | 1 | STA(23.0)-SABc(32.0) | -299 | 10 | 1.0 | 5.0 |
KIHa | 2010 | 3 | 10 | KIHa(83.0)-SABc(28.0) | -250 | 10 | 7.0 | 4.0 |
KIHa | 2010 | 3 | 9 | KIHa(70.5)-RECa(65.5) | -141 | 12 | 5.0 | 6.0 |
KIHa | 2010 | 3 | 8 | CINa(71.0)-KIHa(65.0) | -135 | 5 | 12.0 | 2.0 |
KIHa | 2010 | 3 | 7 | QUAa(55.0)-KIHa(81.0) | -70 | 2 | 15.0 | 0.0 |
KIHa | 2010 | 3 | 6 | KIHa(68.0)-HYAb(68.0) | -90 | 3 | 14.0 | 0.0 |
KIHa | 2010 | 3 | 5 | SABc(86.0)-KIHa(50.0) | -242 | 16 | 1.0 | 8.0 |
KIHa | 2010 | 3 | 4 | RECa(73.0)-KIHa(63.0) | -113 | 5 | 12.0 | 2.0 |
KIHa | 2010 | 3 | 3 | KIHa(67.0)-CINa(69.0) | -289 | 8 | 9.0 | 4.0 |
KIHa | 2010 | 3 | 2 | KIHa(73.0)-QUAa(63.0) | -266 | 11 | 6.0 | 5.0 |
KIHa | 2010 | 3 | 1 | HYAb(61.5)-KIHa(74.5) | -175 | 7 | 10.0 | 3.0 |
KIHa | 2009 | 4 | 10 | YODc(21.0)-KIHa(57.0) | -86 | 3 | 10.0 | 0.0 |
KIHa | 2009 | 4 | 9 | KIHa(57.0)-RECb(21.0) | -117 | 8 | 0.0 | 1.0 |
KIHa | 2009 | 4 | 7 | SABd(25.0)-KIHa(53.0) | -235 | 4 | 9.0 | 1.0 |
KIHb | 2009 | 4 | 6 | PHEb(49.0)-KIHb(29.0) | -203 | 5 | 8.0 | 3.0 |
KIHa | 2009 | 4 | 5 | KIHa(49.5)-YODc(28.5) | -151 | 8 | 5.0 | 2.0 |
KIHa | 2009 | 4 | 3 | YODc(22.0)-KIHa(56.0) | -189 | 3 | 9.5 | 0.0 |
KIHa | 2009 | 4 | 1 | RECb(23.0)-KIHa(55.0) | -147 | 5 | 8.0 | 0.0 |
KIHa | 2008 | 3 | 10 | KIHa(62.0)-RECa(74.0) | -132 | 8 | 9.0 | 4.0 |
KIHb | 2008 | 4 | 9 | KIHb(31.0)-SABd(44.0) | -119 | 2 | 11.0 | 1.0 |
KIHb | 2008 | 4 | 8 | YODc(33.0)-KIHb(45.0) | -140 | 3 | 10.0 | 2.0 |
KIHa | 2008 | 3 | 7 | ACJb(56.0)-KIHa(80.0) | -106 | 6 | 11.0 | 2.0 |
KIHa | 2008 | 3 | 5 | RECa(71.0)-KIHa(65.0) | -82 | 2 | 15.0 | 0.0 |
KIHb | 2008 | 4 | 4 | SABd(43.0)-KIHb(35.0) | -160 | 3 | 10.0 | 2.0 |
KIHa | 2008 | 3 | 3 | SABc(61.0)-KIHa(74.0) | -132 | 8 | 9.0 | 4.0 |
KIHb | 2008 | 4 | 2 | PHEb(46.0)-KIHb(32.0) | -88 | 1 | 12.0 | 0.0 |
KIHb | 2008 | 4 | 1 | KIHb(50.5)-SABd(27.5) | -83 | 1 | 12.0 | 0.0 |
KIHa | 2007 | 4 | 8 | KIHa(48.0)-CINa(30.0) | -161 | 6 | 7.0 | 2.0 |
KIHa | 2007 | 4 | 7 | ACJc(36.0)-KIHa(42.0) | -116 | 4 | 9.0 | 1.0 |
KIHa | 2007 | 4 | 6 | KIHa(56.0)-KIHb(22.0) | -200 | 12 | 0.0 | 5.0 |
KIHa | 2007 | 4 | 5 | KIHa(40.0)-NUPa(38.0) | -236 | 8 | 5.0 | 3.0 |
KIHa | 2007 | 4 | 4 | PHEb(23.0)-KIHa(55.0) | -203 | 13 | 0.0 | 5.0 |
KIHa | 2007 | 4 | 3 | CINa(35.5)-KIHa(42.5) | -131 | 2 | 11.0 | 1.0 |
KIHb | 2007 | 4 | 2 | PHEb(41.5)-KIHb(36.5) | -208 | 2 | 10.5 | 1.5 |
KIHb | 2007 | 4 | 1 | KIHb(21.0)-KIHa(57.0) | -332 | 11 | 4.0 | 8.0 |
HAWa | 2003 | 4 | 10 | SASa(42.0)-HAWa(36.0) | -222 | 10 | 3.0 | 4.0 |
HAWa | 2003 | 4 | 9 | PHEb(39.5)-HAWa(38.5) | -162 | 5 | 7.5 | 2.5 |
HAWa | 2003 | 4 | 8 | HAWa(41.5)-ACJb(36.5) | -256 | 3 | 10.0 | 1.0 |
HAWa | 2003 | 4 | 7 | HAWa(52.0)-KIHb(26.0) | -70 | 2 | 11.0 | 0.0 |
HAWa | 2003 | 4 | 5 | HAWa(35.5)-SASa(42.5) | -117 | 5 | 8.0 | 3.0 |
HAWa | 2003 | 4 | 4 | HAWa(38.0)-PHEb(40.0) | -140 | 4 | 9.0 | 2.0 |
HAWa | 2003 | 4 | 3 | ACJb(48.0)-HAWa(30.0) | -96 | 2 | 11.0 | 1.0 |
HAWa | 2003 | 4 | 2 | KIHb(24.0)-HAWa(54.0) | -142 | 4 | 9.0 | 0.0 |
KIHb | 1999 | 4 | 10 | KIHb(31.0)-SRMa(47.0) | -152 | 3 | 10.0 | 2.0 |
KIHb | 1999 | 4 | 9 | CRQa(47.0)-KIHb(30.0) | -99 | 3 | 10.0 | 2.0 |
KIHb | 1999 | 4 | 7 | KIHb(27.0)-ASSb(51.0) | -93 | 1 | 12.0 | 0.0 |
KIHb | 1999 | 4 | 6 | PHEb(41.0)-KIHb(37.0) | -137 | 2 | 11.0 | 1.0 |
KIHb | 1999 | 4 | 5 | SRMa(49.0)-KIHb(29.0) | -133 | 6 | 7.0 | 4.0 |
KIHb | 1999 | 4 | 4 | KIHb(34.0)-CRQa(44.0) | -114 | 1 | 12.0 | 0.0 |
KIHb | 1999 | 4 | 2 | ASSb(49.0)-KIHb(29.0) | -108 | 1 | 12.0 | 0.0 |
KIHb | 1999 | 4 | 1 | KIHb(47.0)-PHEb(31.0) | -201 | 6 | 7.0 | 2.0 |
KIHa | 1998 | 1 | 11 | ROYa(79.5)-KIHa(55.5) | -60 | 9 | 8.0 | 5.0 |
KIHb | 1998 | 4 | 10 | KIHb(39.0)-HYAb(39.0) | -248 | 6 | 7.0 | 3.0 |
KIHb | 1998 | 4 | 9 | SABd(28.0)-KIHb(50.0) | -189 | 1 | 12.0 | 0.0 |
KIHb | 1998 | 4 | 7 | RECb(32.0)-KIHb(45.0) | -208 | 8 | 5.0 | 3.0 |
KIHb | 1998 | 4 | 6 | KIHb(51.0)-QUAb(27.0) | -51 | 1 | 12.0 | 0.0 |
KIHb | 1998 | 4 | 5 | HYAb(44.0)-KIHb(34.0) | -122 | 6 | 7.0 | 4.0 |
KIHb | 1998 | 4 | 4 | KIHb(45.0)-SABd(33.0) | -71 | 2 | 11.0 | 1.0 |
KIHb | 1998 | 4 | 2 | KIHb(46.0)-RECb(32.0) | -211 | 8 | 5.0 | 3.0 |
KIHb | 1998 | 4 | 1 | QUAb(33.5)-KIHb(44.5) | -141 | 1 | 12.0 | 0.0 |
KIHb | 1997 | 4 | 10 | YODd(23.0)-KIHb(55.0) | -96 | 3 | 10.0 | 0.0 |
KIHb | 1997 | 4 | 9 | KIHb(27.0)-PHEa(51.0) | -140 | 4 | 9.0 | 3.0 |
KIHb | 1997 | 4 | 8 | KAKa(41.0)-KIHb(37.0) | -198 | 8 | 5.0 | 4.0 |
KIHb | 1997 | 4 | 5 | KIHb(53.0)-YODd(26.0) | -132 | 2 | 15.0 | 0.0 |
KIHb | 1997 | 4 | 4 | PHEa(56.0)-KIHb(22.0) | -186 | 13 | 2.0 | 8.0 |
KIHb | 1997 | 4 | 3 | KIHb(47.5)-KAKa(30.5) | -107 | 4 | 9.0 | 1.0 |
KIHb | 1997 | 4 | 2 | SABd(29.0)-KIHb(49.0) | -207 | 10 | 0.0 | 2.0 |
KIHb | 1996 | 4 | 9 | KIHb(84.0)-SASb(52.0) | -150 | 6 | 11.0 | 1.0 |
KIHb | 1996 | 4 | 8 | SRMa(82.0)-KIHb(54.0) | -58 | 4 | 13.0 | 3.0 |
KIHb | 1996 | 4 | 7 | KIHb(82.0)-AMAb(51.0) | -103 | 10 | 7.0 | 3.0 |
KIHb | 1996 | 4 | 5 | KIHb(53.0)-ASSb(83.0) | -162 | 7 | 10.0 | 5.0 |
KIHb | 1996 | 4 | 4 | SASb(51.0)-KIHb(85.0) | -189 | 3 | 14.0 | 0.0 |
KIHb | 1996 | 4 | 3 | KIHb(73.0)-SRMa(63.0) | -119 | 2 | 15.0 | 1.0 |
KIHb | 1996 | 4 | 2 | AMAb(58.0)-KIHb(77.0) | -106 | 2 | 15.0 | 0.0 |
KIHa | 1995 | 2 | 11 | KIHa(70.0)-ACJa(66.0) | -305 | 14 | 3.0 | 7.0 |
KIHb | 1995 | 4 | 8 | KIHb(74.0)-ASSb(61.0) | -35 | 1 | 16.0 | 0.0 |
KIHb | 1995 | 4 | 6 | KIHb(56.0)-AMAa(80.0) | -143 | 11 | 6.0 | 6.0 |
KIHb | 1995 | 4 | 5 | KIHb(92.0)-FUNb(44.0) | -120 | 1 | 16.0 | 0.0 |
KIHb | 1995 | 4 | 4 | SABc(60.0)-KIHb(76.0) | -51 | 1 | 16.0 | 0.0 |
KIHb | 1995 | 4 | 3 | ASSb(80.0)-KIHb(56.0) | -181 | 9 | 8.0 | 6.0 |
KIHb | 1995 | 4 | 1 | AMAa(69.5)-KIHb(66.5) | -182 | 13 | 4.0 | 6.0 |
KIHb | 1994 | 4 | 10 | HELb(82.0)-KIHb(54.0) | -76 | 6 | 11.0 | 4.0 |
KIHb | 1994 | 4 | 9 | KIHb(73.0)-ACJb(63.0) | -88 | 2 | 15.0 | 0.0 |
KIHb | 1994 | 4 | 8 | KIHb(74.0)-SRMa(62.0) | -102 | 4 | 13.0 | 2.0 |
KIHb | 1994 | 4 | 7 | AMAb(59.0)-KIHb(77.0) | -319 | 13 | 4.0 | 6.0 |
KIHa | 1994 | 2 | 6 | CHEa(66.5)-KIHa(69.5) | -190 | 14 | 3.0 | 6.0 |
KIHb | 1994 | 4 | 5 | KIHb(55.0)-HELb(81.0) | -188 | 11 | 6.0 | 6.0 |
KIHb | 1994 | 4 | 4 | ACJb(76.5)-KIHb(59.5) | -186 | 5 | 12.0 | 3.0 |
KIHb | 1994 | 4 | 3 | SRMa(73.0)-KIHb(63.0) | -138 | 5 | 12.0 | 3.0 |
KIHb | 1994 | 4 | 2 | KIHb(78.0)-AMAb(58.0) | -194 | 4 | 13.0 | 1.0 |
KIHb | 1994 | 4 | 1 | CINa(78.0)-KIHb(58.0) | -169 | 3 | 13.5 | 2.0 |
KIHa | 1993 | 2 | 11 | PICa(66.5)-KIHa(69.5) | -129 | 16 | 1.0 | 8.0 |
KIHa | 1993 | 2 | 10 | LOUa(70.0)-KIHa(66.0) | -157 | 13 | 4.0 | 5.0 |
KIHa | 1993 | 2 | 9 | KIHa(76.0)-ACJa(60.0) | -280 | 15 | 2.0 | 7.0 |
KIHa | 1993 | 2 | 8 | KIHa(71.0)-LECa(65.0) | -175 | 14 | 3.0 | 7.0 |
KIHa | 1993 | 2 | 7 | SASa(62.0)-KIHa(74.0) | -185 | 14 | 3.0 | 6.0 |
KIHa | 1993 | 2 | 6 | HYAa(78.0)-KIHa(58.0) | -150 | 15 | 2.0 | 8.0 |
KIHa | 1993 | 2 | 5 | KIHa(81.5)-CHEa(54.5) | -206 | 11 | 6.0 | 3.0 |
KIHa | 1993 | 2 | 4 | KIHa(81.0)-MJAa(55.0) | -330 | 16 | 1.0 | 8.0 |
KIHa | 1993 | 2 | 3 | KIHa(85.0)-SONa(51.0) | -119 | 11 | 6.0 | 4.0 |
KIHa | 1993 | 2 | 2 | CHIa(61.0)-KIHa(75.0) | -261 | 15 | 2.0 | 7.0 |
KIHa | 1993 | 2 | 1 | ASSa(74.0)-KIHa(62.0) | -131 | 14 | 3.0 | 7.0 |
KIHb | 1992 | 4 | 10 | KIHb(76.0)-AMAb(60.0) | -389 | 16 | 1.0 | 8.0 |
KIHa | 1992 | 2 | 9 | MOUa(92.5)-KIHa(43.5) | -81 | 13 | 4.0 | 8.0 |
KIHb | 1992 | 4 | 8 | KIHb(81.0)-CHEb(55.0) | -194 | 2 | 15.0 | 0.0 |
KIHb | 1992 | 4 | 7 | AMAa(66.5)-KIHb(69.5) | -186 | 7 | 10.0 | 3.0 |
KIHa | 1992 | 2 | 6 | KIHa(71.0)-SIRb(65.0) | -268 | 16 | 1.0 | 8.0 |
KIHb | 1992 | 4 | 5 | AMAb(53.0)-KIHb(83.0) | -69 | 1 | 16.0 | 0.0 |
KIHb | 1992 | 4 | 4 | KIHb(79.5)-ANGa(56.5) | -52 | 2 | 15.0 | 1.0 |
KIHb | 1992 | 4 | 3 | CHEb(62.0)-KIHb(74.0) | -166 | 12 | 5.0 | 5.0 |
KIHb | 1992 | 4 | 2 | KIHb(58.0)-AMAa(78.0) | -193 | 8 | 9.0 | 5.0 |
KIHb | 1992 | 4 | 1 | KAKa(66.0)-KIHb(70.0) | -92 | 2 | 15.0 | 1.0 |
KIHb | 1991 | 3 | 10 | MJAa(68.0)-KIHb(68.0) | -107 | 12 | 5.0 | 6.0 |
KIHb | 1991 | 3 | 9 | KIHb(81.0)-SASa(55.0) | -114 | 8 | 9.0 | 2.0 |
KIHb | 1991 | 3 | 8 | SIRc(73.0)-KIHb(63.0) | -83 | 7 | 10.0 | 4.0 |
KIHb | 1991 | 3 | 7 | KIHb(53.0)-SIRb(83.0) | -79 | 7 | 10.0 | 5.0 |
KIHb | 1991 | 3 | 6 | PHOa(76.0)-KIHb(60.0) | -239 | 15 | 2.0 | 7.0 |
KIHb | 1991 | 3 | 5 | KIHb(81.0)-MJAa(55.0) | -51 | 4 | 12.5 | 0.0 |
KIHb | 1991 | 3 | 4 | SASa(91.0)-KIHb(45.0) | -155 | 13 | 4.0 | 8.0 |
KIHb | 1991 | 3 | 3 | KIHb(66.0)-SIRc(70.0) | -129 | 8 | 9.0 | 5.0 |
KIHb | 1991 | 3 | 2 | SIRb(83.5)-KIHb(52.5) | -189 | 14 | 3.0 | 8.0 |
KIHb | 1991 | 3 | 1 | KIHb(80.0)-PHOa(56.0) | -271 | 14 | 3.0 | 7.0 |
KIHb | 1990 | 2 | 11 | KIHb(68.5)-SABb(67.5) | -242 | 15 | 2.0 | 7.0 |
KIHb | 1990 | 2 | 10 | LECa(79.0)-KIHb(57.0) | -103 | 14 | 3.0 | 7.0 |
KIHb | 1990 | 2 | 9 | CHIa(76.5)-KIHb(59.5) | -295 | 12 | 4.5 | 5.5 |
KIHb | 1990 | 2 | 8 | KIHb(44.0)-MOUa(92.0) | -231 | 16 | 1.0 | 8.0 |
KIHb | 1990 | 2 | 7 | SONa(86.5)-KIHb(49.5) | -138 | 11 | 6.0 | 7.0 |
KIHc | 1990 | 4 | 6 | AMAa(53.0)-KIHc(83.0) | -165 | 4 | 13.0 | 1.0 |
KIHb | 1990 | 2 | 5 | KIHb(56.0)-NDPa(80.0) | -154 | 11 | 6.0 | 6.0 |
KIHb | 1990 | 2 | 4 | ASSa(79.0)-KIHb(57.0) | -326 | 16 | 1.0 | 8.0 |
KIHb | 1990 | 2 | 3 | KIHb(55.5)-JAQa(80.5) | -193 | 12 | 5.0 | 7.0 |
KIHb | 1990 | 2 | 2 | OUEb(66.0)-KIHb(70.0) | -203 | 11 | 6.0 | 5.0 |
KIHb | 1990 | 2 | 1 | KIHb(46.0)-KIHa(90.0) | -168 | 15 | 2.0 | 8.0 |
KIHb | 1989 | 3 | 10 | BLOa(68.5)-KIHb(67.5) | -306 | 16 | 1.0 | 8.0 |
KIHb | 1989 | 3 | 9 | KIHb(93.5)-CHEa(42.5) | -130 | 2 | 15.0 | 0.0 |
KIHb | 1989 | 3 | 8 | HYAb(74.0)-KIHb(62.0) | -181 | 13 | 4.0 | 7.0 |
KIHb | 1989 | 3 | 7 | KIHb(89.0)-HELb(47.0) | -76 | 2 | 15.0 | 0.0 |
KIHc | 1989 | 4 | 5 | ACJb(81.0)-KIHc(55.0) | -91 | 3 | 14.0 | 1.0 |
KIHb | 1989 | 3 | 2 | HELb(62.0)-KIHb(74.0) | -142 | 9 | 8.0 | 3.0 |
KIHb | 1989 | 3 | 1 | KIHb(69.0)-ASSb(67.0) | -240 | 16 | 1.0 | 8.0 |
KIHb | 1988 | 3 | 9 | YODa(85.0)-KIHb(51.0) | -245 | 16 | 1.0 | 8.0 |
KIHc | 1988 | 4 | 8 | SASb(73.0)-KIHc(62.0) | -106 | 1 | 16.0 | 0.0 |
KIHb | 1988 | 3 | 7 | BLOa(52.0)-KIHb(84.0) | -221 | 15 | 2.0 | 7.0 |
KIHb | 1988 | 3 | 6 | KIHb(81.0)-CHEa(55.0) | -166 | 7 | 10.0 | 3.0 |
KIHb | 1988 | 3 | 5 | SASa(49.0)-KIHb(87.0) | -191 | 8 | 9.0 | 2.0 |
KIHb | 1988 | 3 | 4 | KIHb(73.0)-YODa(63.0) | -84 | 12 | 5.0 | 5.0 |
KIHb | 1988 | 3 | 3 | ASSb(86.0)-KIHb(50.0) | -93 | 5 | 11.5 | 4.5 |
KIHb | 1988 | 3 | 2 | KIHb(77.5)-BLOa(57.5) | -82 | 5 | 12.0 | 2.0 |
KIHc | 1988 | 4 | 1 | KIHc(64.0)-CINa(72.0) | -177 | 5 | 12.0 | 3.0 |
KIHb | 1987 | 3 | 10 | KIHb(79.0)-CSHa(57.0) | -109 | 5 | 12.0 | 2.0 |
KIHb | 1987 | 3 | 9 | SASa(84.0)-KIHb(52.0) | -265 | 16 | 1.0 | 8.0 |
KIHb | 1987 | 3 | 8 | KIHb(50.0)-ACJa(86.0) | -208 | 14 | 3.0 | 7.0 |
KIHb | 1987 | 3 | 7 | BLOa(58.5)-KIHb(77.5) | -88 | 12 | 5.0 | 5.0 |
KIHb | 1987 | 3 | 6 | KIHb(54.0)-YODa(82.0) | -98 | 15 | 2.0 | 8.0 |
KIHb | 1987 | 3 | 5 | CSHa(53.0)-KIHb(83.0) | -105 | 5 | 12.0 | 1.0 |
KIHb | 1987 | 3 | 4 | KIHb(59.0)-SASa(77.0) | -95 | 4 | 13.0 | 2.0 |
KIHb | 1987 | 3 | 3 | ACJa(97.0)-KIHb(39.0) | -147 | 12 | 5.0 | 8.0 |
KIHc | 1987 | 4 | 2 | ANGa(63.5)-KIHc(72.5) | -83 | 5 | 12.0 | 2.0 |
KIHb | 1987 | 3 | 1 | YODa(81.0)-KIHb(55.0) | -251 | 14 | 3.0 | 7.0 |
KIHb | 1986 | 4 | 9 | KIHb(96.0)-ANGa(40.0) | -149 | 8 | 9.0 | 1.0 |
KIHb | 1986 | 4 | 8 | KAKa(38.0)-KIHb(98.0) | -180 | 9 | 8.0 | 1.0 |
KIHb | 1986 | 4 | 7 | ASSc(74.5)-KIHb(61.5) | -185 | 14 | 3.0 | 7.0 |
KIHb | 1986 | 4 | 6 | KIHb(91.0)-ANGa(45.0) | -117 | 5 | 12.0 | 1.0 |
KIHb | 1986 | 4 | 5 | KIHb(88.0)-KAKa(48.0) | -166 | 8 | 9.0 | 2.0 |
KIHb | 1986 | 4 | 4 | ASSc(61.0)-KIHb(75.0) | -159 | 6 | 11.0 | 2.0 |
KIHb | 1986 | 4 | 3 | ANGa(56.0)-KIHb(80.0) | -193 | 9 | 8.0 | 3.0 |
KIHb | 1986 | 4 | 1 | KIHb(81.5)-ASSc(54.5) | -202 | 9 | 7.5 | 3.5 |
KIHb | 1985 | 4 | 10 | CINa(69.5)-KIHb(66.5) | -251 | 11 | 6.0 | 5.0 |
KIHb | 1985 | 4 | 9 | KIHb(83.0)-SRMa(53.0) | -172 | 3 | 14.0 | 0.0 |
KIHb | 1985 | 4 | 8 | ACJb(59.5)-KIHb(76.5) | -280 | 16 | 1.0 | 8.0 |
KIHb | 1985 | 4 | 7 | KIHb(80.5)-HELb(55.5) | -65 | 7 | 10.0 | 1.0 |
KIHb | 1985 | 4 | 6 | SASa(70.0)-KIHb(66.0) | -271 | 16 | 1.0 | 8.0 |
KIHb | 1985 | 4 | 5 | KIHb(73.0)-CINa(63.0) | -207 | 8 | 9.0 | 3.0 |
KIHb | 1985 | 4 | 4 | SRMa(60.0)-KIHb(76.0) | -301 | 14 | 3.0 | 6.0 |
KIHb | 1985 | 4 | 3 | KIHb(77.0)-ACJb(59.0) | -172 | 15 | 2.0 | 7.0 |
KIHb | 1985 | 4 | 2 | HELb(62.0)-KIHb(74.0) | -132 | 11 | 6.0 | 4.0 |
KIHc | 1984 | 4 | 14 | KIHc(64.0)-HELb(72.0) | -52 | 6 | 11.0 | 2.0 |
KIHc | 1984 | 4 | 13 | SRMa(65.0)-KIHc(71.0) | -217 | 11 | 6.0 | 5.0 |
KIHc | 1984 | 4 | 12 | HELb(79.0)-KIHc(57.0) | -185 | 11 | 6.0 | 6.0 |
KIHc | 1984 | 4 | 11 | KIHc(44.0)-KIHb(92.0) | -201 | 14 | 3.0 | 8.0 |
KIHc | 1984 | 4 | 10 | SASa(88.0)-KIHc(48.0) | -329 | 11 | 6.0 | 7.0 |
KIHc | 1984 | 4 | 9 | CINa(65.5)-KIHc(70.5) | -164 | 6 | 11.0 | 2.0 |
KIHc | 1984 | 4 | 7 | ACJb(81.0)-KIHc(55.0) | -160 | 7 | 10.0 | 4.0 |
KIHc | 1984 | 4 | 6 | KIHc(74.5)-SRMa(61.5) | -182 | 8 | 9.0 | 3.0 |
KIHc | 1984 | 4 | 5 | KIHc(40.0)-SASa(96.0) | -185 | 13 | 4.0 | 8.0 |
KIHc | 1984 | 4 | 2 | KIHc(51.0)-ACJb(85.0) | -398 | 10 | 7.0 | 7.0 |
KIHc | 1984 | 4 | 1 | KIHb(96.0)-KIHc(40.0) | -304 | 9 | 8.0 | 7.0 |
KIHb | 1983 | 3 | 4 | MATb(80.0)-KIHb(55.0) | -322 | 15 | 2.0 | 8.0 |
KIHc | 1982 | 4 | 3 | KIHc(70.0)-PHEc(66.0) | -324 | 16 | 1.0 | 8.0 |