ENST00000344209.10:c.1590G>T
MANE Select
|
ENSP00000345667.5:p.Glu530Asp
|
|
ENST00000460554.2:n.1540G>T
|
|
|
ENST00000642615.1:c.*773G>T
|
ENSP00000495499.1:n.*773G>T
|
|
ENST00000273691.7:c.1458G>T
|
ENSP00000273691.3:p.Glu486Asp
|
|
ENST00000344209.9:c.1590G>T
|
ENSP00000345667.5:p.Glu530Asp
|
|
ENST00000393631.5:c.1323G>T
|
ENSP00000377251.1:p.Glu441Asp
|
|
ENST00000460554.1:n.1692G>T
|
|
|
ENST00000462014.1:c.1494G>T
|
ENSP00000419414.1:p.Glu498Asp
|
|
NM_001199799.1:c.1590G>T
|
NP_001186728.1:p.Glu530Asp
|
|
NM_001199800.1:c.1323G>T
|
NP_001186729.1:p.Glu441Asp
|
|
NM_175924.3:c.1458G>T
|
NP_787120.1:p.Glu486Asp
|
|
XM_005247389.3:c.1494G>T
|
XP_005247446.1:p.Glu498Asp
|
|
XM_011512738.1:c.1558+32G>T
|
XP_011511040.1:n.1558+32G>T
|
|
XM_011512739.1:c.1053G>T
|
XP_011511041.1:p.Glu351Asp
|
|
XM_005247389.4:c.1494G>T
|
XP_005247446.1:p.Glu498Asp
|
|
XM_011512738.2:c.1558+32G>T
|
XP_011511040.1:n.1558+32G>T
|
|
XM_011512739.2:c.1053G>T
|
XP_011511041.1:p.Glu351Asp
|
|
NM_001199799.2:c.1590G>T
MANE Select
|
NP_001186728.1:p.Glu530Asp
|
|
NM_001199800.2:c.1323G>T
|
NP_001186729.1:p.Glu441Asp
|
|
NM_175924.4:c.1458G>T
|
NP_787120.1:p.Glu486Asp
|
|