ENST00000262367.10:c.5212C>T
MANE Select
|
ENSP00000262367.5:p.His1738Tyr
|
|
ENST00000262367.9:c.5212C>T
|
ENSP00000262367.5:p.His1738Tyr
|
|
ENST00000382070.7:c.5098C>T
|
ENSP00000371502.3:p.His1700Tyr
|
|
NM_001079846.1:c.5098C>T
|
NP_001073315.1:p.His1700Tyr
|
|
NM_004380.2:c.5212C>T
|
NP_004371.2:p.His1738Tyr
|
|
XM_005255124.3:c.5167C>T
|
XP_005255181.1:p.His1723Tyr
|
|
XM_005255125.3:c.4795C>T
|
XP_005255182.1:p.His1599Tyr
|
|
XM_006720848.2:c.4951C>T
|
XP_006720911.1:p.His1651Tyr
|
|
XM_011522380.1:c.5158C>T
|
XP_011520682.1:p.His1720Tyr
|
|
XM_011522381.1:c.4459C>T
|
XP_011520683.1:p.His1487Tyr
|
|
XM_005255124.4:c.5167C>T
|
XP_005255181.1:p.His1723Tyr
|
|
XM_005255125.4:c.4795C>T
|
XP_005255182.1:p.His1599Tyr
|
|
XM_006720848.3:c.4951C>T
|
XP_006720911.1:p.His1651Tyr
|
|
XM_011522381.2:c.4459C>T
|
XP_011520683.1:p.His1487Tyr
|
|
XM_017022944.1:c.5206C>T
|
XP_016878433.1:p.His1736Tyr
|
|
NM_004380.3:c.5212C>T
MANE Select
|
NP_004371.2:p.His1738Tyr
|
|