ENST00000585465.3:c.*2860C>A
|
ENSP00000490268.2:n.*2860C>A
|
|
ENST00000585748.3:c.887C>A
|
ENSP00000477641.2:p.Ala296Asp
|
|
ENST00000585851.2:c.1085C>A
|
ENSP00000467912.2:p.Ala362Asp
|
|
ENST00000326873.12:c.1259C>A
MANE Select
|
ENSP00000324856.6:p.Ala420Asp
|
|
ENST00000326873.11:c.1259C>A
|
ENSP00000324856.6:p.Ala420Asp
|
|
ENST00000585465.2:n.2992C>A
|
|
|
ENST00000586243.5:c.1256C>A
|
ENSP00000467240.2:p.Ala419Asp
|
|
ENST00000589152.5:n.1957C>A
|
|
|
NM_000455.4:c.1259C>A , LRG_319t1:c.1259C>A
|
NP_000446.1:p.Ala420Asp
|
|
XM_005259617.1:c.1254C>A
|
XP_005259674.1:p.Arg418=
|
|
XM_011528209.1:c.1032C>A
|
XP_011526511.1:p.Arg344=
|
|
XM_005259617.3:c.1254C>A
|
XP_005259674.1:p.Arg418=
|
|
XM_011528209.2:c.1032C>A
|
XP_011526511.1:p.Arg344=
|
|
XR_001753738.2:n.2065C>A
|
|
|
XR_001753740.2:n.2035C>A
|
|
|
NM_000455.5:c.1259C>A
MANE Select
|
NP_000446.1:p.Ala420Asp
|
|