ENST00000696502.1:c.3834G>T
|
ENSP00000512668.1:p.Glu1278Asp
|
|
ENST00000696503.1:c.3696G>T
|
ENSP00000512669.1:p.Glu1232Asp
|
|
ENST00000696504.1:c.3696G>T
|
ENSP00000512670.1:p.Glu1232Asp
|
|
ENST00000676179.1:c.3771G>T
MANE Select
|
ENSP00000502065.1:p.Glu1257Asp
|
|
ENST00000263934.10:c.3633G>T
|
ENSP00000263934.6:p.Glu1211Asp
|
|
ENST00000377081.5:c.3771G>T
|
ENSP00000366284.1:p.Glu1257Asp
|
|
ENST00000377086.5:c.3771G>T
|
ENSP00000366290.1:p.Glu1257Asp
|
|
ENST00000465635.5:n.226G>T
|
|
|
ENST00000483340.1:n.307G>T
|
|
|
ENST00000620295.2:c.3729G>T
|
ENSP00000478500.1:p.Glu1243Asp
|
|
ENST00000622724.3:c.3693G>T
|
ENSP00000480063.1:p.Glu1231Asp
|
|
NM_015074.3:c.3633G>T , LRG_252t1:c.3633G>T
|
NP_055889.2:p.Glu1211Asp
|
|
NM_001365951.1:c.3771G>T
|
NP_001352880.1:p.Glu1257Asp
|
|
NM_001365952.1:c.3771G>T
|
NP_001352881.1:p.Glu1257Asp
|
|
NM_001365951.3:c.3771G>T
MANE Select
|
NP_001352880.1:p.Glu1257Asp
|
|