ENST00000262367.10:c.5498G>T
MANE Select
|
ENSP00000262367.5:p.Cys1833Phe
|
|
ENST00000262367.9:c.5498G>T
|
ENSP00000262367.5:p.Cys1833Phe
|
|
ENST00000382070.7:c.5384G>T
|
ENSP00000371502.3:p.Cys1795Phe
|
|
NM_001079846.1:c.5384G>T
|
NP_001073315.1:p.Cys1795Phe
|
|
NM_004380.2:c.5498G>T
|
NP_004371.2:p.Cys1833Phe
|
|
XM_005255124.3:c.5453G>T
|
XP_005255181.1:p.Cys1818Phe
|
|
XM_005255125.3:c.5081G>T
|
XP_005255182.1:p.Cys1694Phe
|
|
XM_006720848.2:c.5237G>T
|
XP_006720911.1:p.Cys1746Phe
|
|
XM_011522380.1:c.5444G>T
|
XP_011520682.1:p.Cys1815Phe
|
|
XM_011522381.1:c.4745G>T
|
XP_011520683.1:p.Cys1582Phe
|
|
XM_005255124.4:c.5453G>T
|
XP_005255181.1:p.Cys1818Phe
|
|
XM_005255125.4:c.5081G>T
|
XP_005255182.1:p.Cys1694Phe
|
|
XM_006720848.3:c.5237G>T
|
XP_006720911.1:p.Cys1746Phe
|
|
XM_011522381.2:c.4745G>T
|
XP_011520683.1:p.Cys1582Phe
|
|
XM_017022944.1:c.5492G>T
|
XP_016878433.1:p.Cys1831Phe
|
|
NM_004380.3:c.5498G>T
MANE Select
|
NP_004371.2:p.Cys1833Phe
|
|