ENST00000471318.6:n.943G>C
|
|
|
ENST00000621467.5:c.1021G>C
|
ENSP00000480508.2:p.Asp341His
|
|
ENST00000686475.1:n.1087G>C
|
|
|
ENST00000409883.7:c.1147G>C
MANE Select
|
ENSP00000386264.2:p.Asp383His
|
|
ENST00000286196.9:c.*711G>C
|
ENSP00000286196.5:n.*711G>C
|
|
ENST00000409444.6:c.1123G>C
|
ENSP00000387203.2:p.Asp375His
|
|
ENST00000409883.6:c.1147G>C
|
ENSP00000386264.2:p.Asp383His
|
|
ENST00000471318.5:n.375G>C
|
|
|
ENST00000495329.1:n.286G>C
|
|
|
ENST00000621467.4:c.1123G>C
|
ENSP00000480508.1:p.Asp375His
|
|
NM_001044385.2:c.1147G>C
|
NP_001037850.1:p.Asp383His
|
|
NM_152388.3:c.1123G>C
|
NP_689601.2:p.Asp375His
|
|
NM_001044385.3:c.1147G>C
MANE Select
|
NP_001037850.1:p.Asp383His
|
|
NM_152388.4:c.1123G>C
|
NP_689601.2:p.Asp375His
|
|