|
ENST00000381129.8:c.715T>C
MANE Select
|
ENSP00000370521.3:p.Cys239Arg
|
|
|
ENST00000250087.9:c.526T>C
|
ENSP00000250087.5:p.Cys176Arg
|
|
|
ENST00000381128.2:c.*587T>C
|
ENSP00000370520.2:n.*587T>C
|
|
|
ENST00000381129.7:c.715T>C
|
ENSP00000370521.3:p.Cys239Arg
|
|
|
ENST00000570466.5:c.649T>C
|
ENSP00000461287.1:p.Cys217Arg
|
|
|
ENST00000570584.5:c.251+7235T>C
|
|
|
|
ENST00000571740.5:c.691T>C
|
ENSP00000460134.1:p.Cys231Arg
|
|
|
ENST00000574506.5:c.679T>C
|
ENSP00000458456.1:p.Cys227Arg
|
|
|
ENST00000575265.5:c.715T>C
|
ENSP00000459673.1:p.Cys239Arg
|
|
|
ENST00000576307.5:c.535T>C
|
ENSP00000459522.1:p.Cys179Arg
|
|
|
ENST00000576776.5:c.643T>C
|
ENSP00000460827.1:p.Cys215Arg
|
|
|
ENST00000621374.4:c.715T>C
|
ENSP00000481337.1:p.Cys239Arg
|
|
|
NM_001033054.2:c.526T>C
|
NP_001028226.1:p.Cys176Arg
|
|
|
NM_001033055.2:c.535T>C
|
NP_001028227.1:p.Cys179Arg
|
|
|
NM_001285399.2:c.679T>C
|
NP_001272328.1:p.Cys227Arg
|
|
|
NM_001285400.2:c.649T>C
|
NP_001272329.1:p.Cys217Arg
|
|
|
NM_001285401.2:c.643T>C
|
NP_001272330.1:p.Cys215Arg
|
|
|
NM_001285402.1:c.598T>C
|
NP_001272331.1:p.Cys200Arg
|
|
|
NM_001285403.2:c.691T>C
|
NP_001272332.1:p.Cys231Arg
|
|
|
NM_014336.4:c.715T>C
|
NP_055151.3:p.Cys239Arg
|
|
|
NM_001033054.3:c.526T>C
|
NP_001028226.1:p.Cys176Arg
|
|
|
NM_001033055.3:c.535T>C
|
NP_001028227.1:p.Cys179Arg
|
|
|
NM_001285399.3:c.679T>C
|
NP_001272328.1:p.Cys227Arg
|
|
|
NM_001285400.3:c.649T>C
|
NP_001272329.1:p.Cys217Arg
|
|
|
NM_001285401.3:c.643T>C
|
NP_001272330.1:p.Cys215Arg
|
|
|
NM_001285402.2:c.598T>C
|
NP_001272331.1:p.Cys200Arg
|
|
|
NM_001285403.3:c.691T>C
|
NP_001272332.1:p.Cys231Arg
|
|
|
NM_014336.5:c.715T>C
MANE Select
|
NP_055151.3:p.Cys239Arg
|
|
|
NM_001285403.4:c.691T>C
|
NP_001272332.1:p.Cys231Arg
|
|
