NM_004364.5:c.1071C>G
MANE Select
|
NP_004355.2:p.Cys357Trp
|
ENST00000498907.3:c.1071C>G
MANE Select
|
ENSP00000427514.1:p.Cys357Trp
|
NM_001285829.1:c.714C>G
|
NP_001272758.1:p.Cys238Trp
|
NM_001285829.2:c.714C>G
|
NP_001272758.1:p.Cys238Trp
|
NM_001287424.1:c.1176C>G
|
NP_001274353.1:p.Cys392Trp
|
NM_001287424.2:c.1176C>G
|
NP_001274353.1:p.Cys392Trp
|
NM_001287435.1:c.1029C>G
|
NP_001274364.1:p.Cys343Trp
|
NM_001287435.2:c.1029C>G
|
NP_001274364.1:p.Cys343Trp
|
NM_004364.4:c.1071C>G
|
NP_004355.2:p.Cys357Trp
|
ENST00000498907.2:c.1071C>G
|
ENSP00000427514.1:p.Cys357Trp
|