ENST00000471318.6:n.954A>G
|
|
|
ENST00000621467.5:c.1032A>G
|
ENSP00000480508.2:p.Glu344=
|
|
ENST00000686475.1:n.1098A>G
|
|
|
ENST00000409883.7:c.1158A>G
MANE Select
|
ENSP00000386264.2:p.Glu386=
|
|
ENST00000286196.9:c.*722A>G
|
ENSP00000286196.5:n.*722A>G
|
|
ENST00000409444.6:c.1134A>G
|
ENSP00000387203.2:p.Glu378=
|
|
ENST00000409883.6:c.1158A>G
|
ENSP00000386264.2:p.Glu386=
|
|
ENST00000471318.5:n.386A>G
|
|
|
ENST00000495329.1:n.297A>G
|
|
|
ENST00000621467.4:c.1134A>G
|
ENSP00000480508.1:p.Glu378=
|
|
NM_001044385.2:c.1158A>G
|
NP_001037850.1:p.Glu386=
|
|
NM_152388.3:c.1134A>G
|
NP_689601.2:p.Glu378=
|
|
NM_001044385.3:c.1158A>G
MANE Select
|
NP_001037850.1:p.Glu386=
|
|
NM_152388.4:c.1134A>G
|
NP_689601.2:p.Glu378=
|
|