ENST00000471318.6:n.953A>T
|
|
|
ENST00000621467.5:c.1031A>T
|
ENSP00000480508.2:p.Glu344Val
|
|
ENST00000686475.1:n.1097A>T
|
|
|
ENST00000409883.7:c.1157A>T
MANE Select
|
ENSP00000386264.2:p.Glu386Val
|
|
ENST00000286196.9:c.*721A>T
|
ENSP00000286196.5:n.*721A>T
|
|
ENST00000409444.6:c.1133A>T
|
ENSP00000387203.2:p.Glu378Val
|
|
ENST00000409883.6:c.1157A>T
|
ENSP00000386264.2:p.Glu386Val
|
|
ENST00000471318.5:n.385A>T
|
|
|
ENST00000495329.1:n.296A>T
|
|
|
ENST00000621467.4:c.1133A>T
|
ENSP00000480508.1:p.Glu378Val
|
|
NM_001044385.2:c.1157A>T
|
NP_001037850.1:p.Glu386Val
|
|
NM_152388.3:c.1133A>T
|
NP_689601.2:p.Glu378Val
|
|
NM_001044385.3:c.1157A>T
MANE Select
|
NP_001037850.1:p.Glu386Val
|
|
NM_152388.4:c.1133A>T
|
NP_689601.2:p.Glu378Val
|
|