ENST00000262367.10:c.7078C>T
MANE Select
|
ENSP00000262367.5:p.His2360Tyr
|
|
ENST00000262367.9:c.7078C>T
|
ENSP00000262367.5:p.His2360Tyr
|
|
ENST00000382070.7:c.6964C>T
|
ENSP00000371502.3:p.His2322Tyr
|
|
NM_001079846.1:c.6964C>T
|
NP_001073315.1:p.His2322Tyr
|
|
NM_004380.2:c.7078C>T
|
NP_004371.2:p.His2360Tyr
|
|
XM_005255124.3:c.7033C>T
|
XP_005255181.1:p.His2345Tyr
|
|
XM_005255125.3:c.6661C>T
|
XP_005255182.1:p.His2221Tyr
|
|
XM_006720848.2:c.6817C>T
|
XP_006720911.1:p.His2273Tyr
|
|
XM_011522380.1:c.7024C>T
|
XP_011520682.1:p.His2342Tyr
|
|
XM_011522381.1:c.6325C>T
|
XP_011520683.1:p.His2109Tyr
|
|
XM_005255124.4:c.7033C>T
|
XP_005255181.1:p.His2345Tyr
|
|
XM_005255125.4:c.6661C>T
|
XP_005255182.1:p.His2221Tyr
|
|
XM_006720848.3:c.6817C>T
|
XP_006720911.1:p.His2273Tyr
|
|
XM_011522381.2:c.6325C>T
|
XP_011520683.1:p.His2109Tyr
|
|
XM_017022944.1:c.7072C>T
|
XP_016878433.1:p.His2358Tyr
|
|
NM_004380.3:c.7078C>T
MANE Select
|
NP_004371.2:p.His2360Tyr
|
|