ENST00000585465.3:c.*2847A>G
|
ENSP00000490268.2:n.*2847A>G
|
|
ENST00000585748.3:c.874A>G
|
ENSP00000477641.2:p.Lys292Glu
|
|
ENST00000585851.2:c.1072A>G
|
ENSP00000467912.2:p.Lys358Glu
|
|
ENST00000326873.12:c.1246A>G
MANE Select
|
ENSP00000324856.6:p.Lys416Glu
|
|
ENST00000326873.11:c.1246A>G
|
ENSP00000324856.6:p.Lys416Glu
|
|
ENST00000585465.2:n.2979A>G
|
|
|
ENST00000586243.5:c.1245A>G
|
ENSP00000467240.2:p.Ala415=
|
|
ENST00000589152.5:n.1944A>G
|
|
|
NM_000455.4:c.1246A>G , LRG_319t1:c.1246A>G
|
NP_000446.1:p.Lys416Glu
|
|
XM_005259617.1:c.1241A>G
|
XP_005259674.1:p.Gln414Arg
|
|
XM_011528209.1:c.1019A>G
|
XP_011526511.1:p.Gln340Arg
|
|
XM_005259617.3:c.1241A>G
|
XP_005259674.1:p.Gln414Arg
|
|
XM_011528209.2:c.1019A>G
|
XP_011526511.1:p.Gln340Arg
|
|
XR_001753738.2:n.2052A>G
|
|
|
XR_001753740.2:n.2022A>G
|
|
|
NM_000455.5:c.1246A>G
MANE Select
|
NP_000446.1:p.Lys416Glu
|
|