ENST00000585465.3:c.*2794C=
|
ENSP00000490268.2:n.*2794C=
|
|
ENST00000585748.3:c.821C=
|
ENSP00000477641.2:p.Ala274=
|
|
ENST00000585851.2:c.1019C=
|
ENSP00000467912.2:p.Ala340=
|
|
ENST00000326873.12:c.1193C=
MANE Select
|
ENSP00000324856.6:p.Ala398=
|
|
ENST00000326873.11:c.1193C=
|
ENSP00000324856.6:p.Ala398=
|
|
ENST00000585465.2:n.2926C=
|
|
|
ENST00000586243.5:c.1193C=
|
ENSP00000467240.2:p.Ala398=
|
|
ENST00000589152.5:n.1891C=
|
|
|
NM_000455.4:c.1193C= , LRG_319t1:c.1193C=
|
NP_000446.1:p.Ala398=
|
|
XM_005259617.1:c.1188C=
|
XP_005259674.1:p.Gly396=
|
|
XM_011528209.1:c.966C=
|
XP_011526511.1:p.Gly322=
|
|
XM_005259617.3:c.1188C=
|
XP_005259674.1:p.Gly396=
|
|
XM_011528209.2:c.966C=
|
XP_011526511.1:p.Gly322=
|
|
XR_001753738.2:n.1999C=
|
|
|
XR_001753740.2:n.1969C=
|
|
|
NM_000455.5:c.1193C=
MANE Select
|
NP_000446.1:p.Ala398=
|
|