ENST00000262367.10:c.4532T>G
MANE Select
|
ENSP00000262367.5:p.Phe1511Cys
|
|
ENST00000262367.9:c.4532T>G
|
ENSP00000262367.5:p.Phe1511Cys
|
|
ENST00000382070.7:c.4418T>G
|
ENSP00000371502.3:p.Phe1473Cys
|
|
ENST00000570939.2:c.3167T>G
|
ENSP00000461002.2:p.Phe1056Cys
|
|
ENST00000571763.5:n.322T>G
|
|
|
ENST00000574740.1:n.353T>G
|
|
|
ENST00000576720.1:n.3355T>G
|
|
|
NM_001079846.1:c.4418T>G
|
NP_001073315.1:p.Phe1473Cys
|
|
NM_004380.2:c.4532T>G
|
NP_004371.2:p.Phe1511Cys
|
|
XM_005255124.3:c.4487T>G
|
XP_005255181.1:p.Phe1496Cys
|
|
XM_005255125.3:c.4115T>G
|
XP_005255182.1:p.Phe1372Cys
|
|
XM_006720848.2:c.4271T>G
|
XP_006720911.1:p.Phe1424Cys
|
|
XM_011522380.1:c.4478T>G
|
XP_011520682.1:p.Phe1493Cys
|
|
XM_011522381.1:c.3779T>G
|
XP_011520683.1:p.Phe1260Cys
|
|
XM_005255124.4:c.4487T>G
|
XP_005255181.1:p.Phe1496Cys
|
|
XM_005255125.4:c.4115T>G
|
XP_005255182.1:p.Phe1372Cys
|
|
XM_006720848.3:c.4271T>G
|
XP_006720911.1:p.Phe1424Cys
|
|
XM_011522381.2:c.3779T>G
|
XP_011520683.1:p.Phe1260Cys
|
|
XM_017022944.1:c.4526T>G
|
XP_016878433.1:p.Phe1509Cys
|
|
NM_004380.3:c.4532T>G
MANE Select
|
NP_004371.2:p.Phe1511Cys
|
|