ENST00000585465.3:c.*2724G=
|
ENSP00000490268.2:n.*2724G=
|
|
ENST00000585748.3:c.751G=
|
ENSP00000477641.2:p.Glu251=
|
|
ENST00000585851.2:c.949G=
|
ENSP00000467912.2:p.Glu317=
|
|
ENST00000326873.12:c.1123G=
MANE Select
|
ENSP00000324856.6:p.Glu375=
|
|
ENST00000326873.11:c.1123G=
|
ENSP00000324856.6:p.Glu375=
|
|
ENST00000585465.2:n.2856G=
|
|
|
ENST00000586243.5:c.1123G=
|
ENSP00000467240.2:p.Glu375=
|
|
ENST00000589152.5:n.1821G=
|
|
|
NM_000455.4:c.1123G= , LRG_319t1:c.1123G=
|
NP_000446.1:p.Glu375=
|
|
XM_005259617.1:c.1118G=
|
XP_005259674.1:p.Arg373=
|
|
XM_011528209.1:c.896G=
|
XP_011526511.1:p.Arg299=
|
|
XM_005259617.3:c.1118G=
|
XP_005259674.1:p.Arg373=
|
|
XM_011528209.2:c.896G=
|
XP_011526511.1:p.Arg299=
|
|
XR_001753738.2:n.1929G=
|
|
|
XR_001753740.2:n.1899G=
|
|
|
NM_000455.5:c.1123G=
MANE Select
|
NP_000446.1:p.Glu375=
|
|