ENST00000585465.3:c.*2789G>C
|
ENSP00000490268.2:n.*2789G>C
|
|
ENST00000585748.3:c.816G>C
|
ENSP00000477641.2:p.Glu272Asp
|
|
ENST00000585851.2:c.1014G>C
|
ENSP00000467912.2:p.Glu338Asp
|
|
ENST00000326873.12:c.1188G>C
MANE Select
|
ENSP00000324856.6:p.Glu396Asp
|
|
ENST00000326873.11:c.1188G>C
|
ENSP00000324856.6:p.Glu396Asp
|
|
ENST00000585465.2:n.2921G>C
|
|
|
ENST00000586243.5:c.1188G>C
|
ENSP00000467240.2:p.Glu396Asp
|
|
ENST00000589152.5:n.1886G>C
|
|
|
NM_000455.4:c.1188G>C , LRG_319t1:c.1188G>C
|
NP_000446.1:p.Glu396Asp
|
|
XM_005259617.1:c.1183G>C
|
XP_005259674.1:p.Gly395Arg
|
|
XM_011528209.1:c.961G>C
|
XP_011526511.1:p.Gly321Arg
|
|
XM_005259617.3:c.1183G>C
|
XP_005259674.1:p.Gly395Arg
|
|
XM_011528209.2:c.961G>C
|
XP_011526511.1:p.Gly321Arg
|
|
XR_001753738.2:n.1994G>C
|
|
|
XR_001753740.2:n.1964G>C
|
|
|
NM_000455.5:c.1188G>C
MANE Select
|
NP_000446.1:p.Glu396Asp
|
|