ENST00000262367.10:c.4457G>A
MANE Select
|
ENSP00000262367.5:p.Cys1486Tyr
|
|
ENST00000262367.9:c.4457G>A
|
ENSP00000262367.5:p.Cys1486Tyr
|
|
ENST00000382070.7:c.4343G>A
|
ENSP00000371502.3:p.Cys1448Tyr
|
|
ENST00000570939.2:c.3092G>A
|
ENSP00000461002.2:p.Cys1031Tyr
|
|
ENST00000571763.5:n.247G>A
|
|
|
ENST00000574740.1:n.278G>A
|
|
|
ENST00000576720.1:n.3280G>A
|
|
|
NM_001079846.1:c.4343G>A
|
NP_001073315.1:p.Cys1448Tyr
|
|
NM_004380.2:c.4457G>A
|
NP_004371.2:p.Cys1486Tyr
|
|
XM_005255124.3:c.4412G>A
|
XP_005255181.1:p.Cys1471Tyr
|
|
XM_005255125.3:c.4040G>A
|
XP_005255182.1:p.Cys1347Tyr
|
|
XM_006720848.2:c.4196G>A
|
XP_006720911.1:p.Cys1399Tyr
|
|
XM_011522380.1:c.4403G>A
|
XP_011520682.1:p.Cys1468Tyr
|
|
XM_011522381.1:c.3704G>A
|
XP_011520683.1:p.Cys1235Tyr
|
|
XM_005255124.4:c.4412G>A
|
XP_005255181.1:p.Cys1471Tyr
|
|
XM_005255125.4:c.4040G>A
|
XP_005255182.1:p.Cys1347Tyr
|
|
XM_006720848.3:c.4196G>A
|
XP_006720911.1:p.Cys1399Tyr
|
|
XM_011522381.2:c.3704G>A
|
XP_011520683.1:p.Cys1235Tyr
|
|
XM_017022944.1:c.4451G>A
|
XP_016878433.1:p.Cys1484Tyr
|
|
NM_004380.3:c.4457G>A
MANE Select
|
NP_004371.2:p.Cys1486Tyr
|
|