ENST00000265641.10:c.-14+6086G>T
MANE Select
|
ENSP00000265641.4:n.-14+6086G>T
|
|
ENST00000265641.9:c.-14+6086G>T
|
ENSP00000265641.4:n.-14+6086G>T
|
|
ENST00000376618.6:c.-14+6086G>T
|
ENSP00000365803.2:n.-14+6086G>T
|
|
ENST00000561996.1:c.-14+8456G>T
|
ENSP00000457663.1:n.-14+8456G>T
|
|
ENST00000569129.5:c.-14+3863G>T
|
ENSP00000455116.1:n.-14+3863G>T
|
|
NM_001031847.2:c.-14+6086G>T
|
NP_001027017.1:n.-14+6086G>T
|
|
NM_001876.3:c.-14+6086G>T
|
NP_001867.2:n.-14+6086G>T
|
|
XM_005273762.1:c.83+3863G>T
|
XP_005273819.1:n.83+3863G>T
|
|
XM_005273763.1:c.83+3863G>T
|
XP_005273820.1:n.83+3863G>T
|
|
XM_005273762.3:c.83+3863G>T
|
XP_005273819.1:n.83+3863G>T
|
|
XM_017017220.1:c.-14+8456G>T
|
XP_016872709.1:n.-14+8456G>T
|
|
NM_001876.4:c.-14+6086G>T
MANE Select
|
NP_001867.2:n.-14+6086G>T
|
|
NM_001031847.3:c.-14+6086G>T
|
NP_001027017.1:n.-14+6086G>T
|
|