ENST00000262367.10:c.4397A>G
MANE Select
|
ENSP00000262367.5:p.Tyr1466Cys
|
|
ENST00000262367.9:c.4397A>G
|
ENSP00000262367.5:p.Tyr1466Cys
|
|
ENST00000382070.7:c.4283A>G
|
ENSP00000371502.3:p.Tyr1428Cys
|
|
ENST00000570939.2:c.3032A>G
|
ENSP00000461002.2:p.Tyr1011Cys
|
|
ENST00000571763.5:n.187A>G
|
|
|
ENST00000574740.1:n.218A>G
|
|
|
ENST00000576720.1:n.3220A>G
|
|
|
NM_001079846.1:c.4283A>G
|
NP_001073315.1:p.Tyr1428Cys
|
|
NM_004380.2:c.4397A>G
|
NP_004371.2:p.Tyr1466Cys
|
|
XM_005255124.3:c.4352A>G
|
XP_005255181.1:p.Tyr1451Cys
|
|
XM_005255125.3:c.3980A>G
|
XP_005255182.1:p.Tyr1327Cys
|
|
XM_006720848.2:c.4136A>G
|
XP_006720911.1:p.Tyr1379Cys
|
|
XM_011522380.1:c.4343A>G
|
XP_011520682.1:p.Tyr1448Cys
|
|
XM_011522381.1:c.3644A>G
|
XP_011520683.1:p.Tyr1215Cys
|
|
XM_005255124.4:c.4352A>G
|
XP_005255181.1:p.Tyr1451Cys
|
|
XM_005255125.4:c.3980A>G
|
XP_005255182.1:p.Tyr1327Cys
|
|
XM_006720848.3:c.4136A>G
|
XP_006720911.1:p.Tyr1379Cys
|
|
XM_011522381.2:c.3644A>G
|
XP_011520683.1:p.Tyr1215Cys
|
|
XM_017022944.1:c.4391A>G
|
XP_016878433.1:p.Tyr1464Cys
|
|
NM_004380.3:c.4397A>G
MANE Select
|
NP_004371.2:p.Tyr1466Cys
|
|