ENST00000703783.1:n.1016A>T
|
|
|
ENST00000703785.1:n.1097A>T
|
|
|
ENST00000262464.9:c.4232A>T
MANE Select
|
ENSP00000262464.4:p.Glu1411Val
|
|
ENST00000262464.8:c.4232A>T
|
ENSP00000262464.4:p.Glu1411Val
|
|
ENST00000507835.5:c.782A>T
|
ENSP00000426839.1:p.Glu261Val
|
|
ENST00000508053.5:c.4232A>T
|
ENSP00000424571.1:p.Glu1411Val
|
|
ENST00000508989.5:c.4133A>T
|
ENSP00000425596.1:p.Glu1378Val
|
|
ENST00000619499.4:c.4229A>T
|
ENSP00000482132.1:p.Glu1410Val
|
|
NM_001999.3:c.4232A>T
|
NP_001990.2:p.Glu1411Val
|
|
XM_017009228.2:c.4079A>T
|
XP_016864717.1:p.Glu1360Val
|
|
NM_001999.4:c.4232A>T
MANE Select
|
NP_001990.2:p.Glu1411Val
|
|