ENST00000262367.10:c.3596G>A
MANE Select
|
ENSP00000262367.5:p.Cys1199Tyr
|
|
ENST00000262367.9:c.3596G>A
|
ENSP00000262367.5:p.Cys1199Tyr
|
|
ENST00000382070.7:c.3482G>A
|
ENSP00000371502.3:p.Cys1161Tyr
|
|
ENST00000570939.2:c.2201G>A
|
ENSP00000461002.2:p.Cys734Tyr
|
|
NM_001079846.1:c.3482G>A
|
NP_001073315.1:p.Cys1161Tyr
|
|
NM_004380.2:c.3596G>A
|
NP_004371.2:p.Cys1199Tyr
|
|
XM_005255124.3:c.3551G>A
|
XP_005255181.1:p.Cys1184Tyr
|
|
XM_005255125.3:c.3179G>A
|
XP_005255182.1:p.Cys1060Tyr
|
|
XM_006720848.2:c.3596G>A
|
XP_006720911.1:p.Cys1199Tyr
|
|
XM_011522380.1:c.3542G>A
|
XP_011520682.1:p.Cys1181Tyr
|
|
XM_011522381.1:c.2843G>A
|
XP_011520683.1:p.Cys948Tyr
|
|
XM_011522382.1:c.3596G>A
|
XP_011520684.1:p.Cys1199Tyr
|
|
XM_005255124.4:c.3551G>A
|
XP_005255181.1:p.Cys1184Tyr
|
|
XM_005255125.4:c.3179G>A
|
XP_005255182.1:p.Cys1060Tyr
|
|
XM_006720848.3:c.3596G>A
|
XP_006720911.1:p.Cys1199Tyr
|
|
XM_011522381.2:c.2843G>A
|
XP_011520683.1:p.Cys948Tyr
|
|
XM_011522382.3:c.3596G>A
|
XP_011520684.1:p.Cys1199Tyr
|
|
XM_017022944.1:c.3590G>A
|
XP_016878433.1:p.Cys1197Tyr
|
|
NM_004380.3:c.3596G>A
MANE Select
|
NP_004371.2:p.Cys1199Tyr
|
|