ENST00000289575.10:c.1465T>C
MANE Select
|
ENSP00000289575.5:p.Cys489Arg
|
|
ENST00000289575.9:c.1465T>C
|
ENSP00000289575.5:p.Cys489Arg
|
|
ENST00000428359.6:c.1399T>C
|
ENSP00000388912.2:p.Cys467Arg
|
|
ENST00000454962.6:c.784T>C
|
ENSP00000389653.2:p.Cys262Arg
|
|
ENST00000525650.5:c.1033T>C
|
ENSP00000436324.1:p.Cys345Arg
|
|
ENST00000528108.1:n.271T>C
|
|
|
ENST00000530012.1:n.292T>C
|
|
|
ENST00000531756.5:n.1012T>C
|
|
|
ENST00000532236.5:c.1117T>C
|
ENSP00000434112.1:p.Cys373Arg
|
|
NM_001145211.2:c.1399T>C
|
NP_001138683.1:p.Cys467Arg
|
|
NM_001145212.2:c.1033T>C
|
NP_001138684.1:p.Cys345Arg
|
|
NM_007256.4:c.1465T>C
|
NP_009187.1:p.Cys489Arg
|
|
XM_017017157.1:c.1471T>C
|
XP_016872646.1:p.Cys491Arg
|
|
NM_001145211.3:c.1399T>C
|
NP_001138683.1:p.Cys467Arg
|
|
NM_001145212.3:c.1033T>C
|
NP_001138684.1:p.Cys345Arg
|
|
NM_007256.5:c.1465T>C
MANE Select
|
NP_009187.1:p.Cys489Arg
|
|