ENST00000585465.3:c.*2864C>G
|
ENSP00000490268.2:n.*2864C>G
|
|
ENST00000585748.3:c.891C>G
|
ENSP00000477641.2:p.Ser297Arg
|
|
ENST00000585851.2:c.1089C>G
|
ENSP00000467912.2:p.Ser363Arg
|
|
ENST00000326873.12:c.1263C>G
MANE Select
|
ENSP00000324856.6:p.Ser421Arg
|
|
ENST00000326873.11:c.1263C>G
|
ENSP00000324856.6:p.Ser421Arg
|
|
ENST00000585465.2:n.2996C>G
|
|
|
ENST00000586243.5:c.1260C>G
|
ENSP00000467240.2:p.Ser420Arg
|
|
ENST00000589152.5:n.1961C>G
|
|
|
NM_000455.4:c.1263C>G , LRG_319t1:c.1263C>G
|
NP_000446.1:p.Ser421Arg
|
|
XM_005259617.1:c.1258C>G
|
XP_005259674.1:p.Gln420Glu
|
|
XM_011528209.1:c.1036C>G
|
XP_011526511.1:p.Gln346Glu
|
|
XM_005259617.3:c.1258C>G
|
XP_005259674.1:p.Gln420Glu
|
|
XM_011528209.2:c.1036C>G
|
XP_011526511.1:p.Gln346Glu
|
|
XR_001753738.2:n.2069C>G
|
|
|
XR_001753740.2:n.2039C>G
|
|
|
NM_000455.5:c.1263C>G
MANE Select
|
NP_000446.1:p.Ser421Arg
|
|