ENST00000264414.9:c.1250T>A
MANE Select
|
ENSP00000264414.4:p.Val417Asp
|
|
ENST00000264414.8:c.1250T>A
|
ENSP00000264414.4:p.Val417Asp
|
|
ENST00000344951.8:c.1052T>A
|
ENSP00000343601.4:p.Val351Asp
|
|
ENST00000409096.5:c.1178T>A
|
ENSP00000387200.1:p.Val393Asp
|
|
ENST00000409777.5:c.1178T>A
|
ENSP00000386525.1:p.Val393Asp
|
|
ENST00000481135.1:n.546T>A
|
|
|
ENST00000617432.4:c.-27T>A
|
ENSP00000477851.1:n.-27T>A
|
|
NM_001257197.1:c.1052T>A
|
NP_001244126.1:p.Val351Asp
|
|
NM_001257198.1:c.1268T>A
|
NP_001244127.1:p.Val423Asp
|
|
NM_003590.4:c.1250T>A
|
NP_003581.1:p.Val417Asp
|
|
XM_006712800.2:c.1217T>A
|
XP_006712863.2:p.Val406Asp
|
|
XM_011511994.1:c.1103T>A
|
XP_011510296.1:p.Val368Asp
|
|
XM_011511995.1:c.1208T>A
|
XP_011510297.1:p.Val403Asp
|
|
XM_011511996.1:c.1058T>A
|
XP_011510298.1:p.Val353Asp
|
|
XM_011511997.1:c.950T>A
|
XP_011510299.1:p.Val317Asp
|
|
XM_011511994.3:c.1103T>A
|
XP_011510296.1:p.Val368Asp
|
|
XM_011511996.2:c.1058T>A
|
XP_011510298.1:p.Val353Asp
|
|
NM_003590.5:c.1250T>A
MANE Select
|
NP_003581.1:p.Val417Asp
|
|
NM_001257198.2:c.1268T>A
|
NP_001244127.1:p.Val423Asp
|
|
NM_001257197.2:c.1052T>A
|
NP_001244126.1:p.Val351Asp
|
|