ENST00000262367.10:c.2611C>T
MANE Select
|
ENSP00000262367.5:p.His871Tyr
|
|
ENST00000262367.9:c.2611C>T
|
ENSP00000262367.5:p.His871Tyr
|
|
ENST00000382070.7:c.2497C>T
|
ENSP00000371502.3:p.His833Tyr
|
|
ENST00000570939.2:c.1216C>T
|
ENSP00000461002.2:p.His406Tyr
|
|
NM_001079846.1:c.2497C>T
|
NP_001073315.1:p.His833Tyr
|
|
NM_004380.2:c.2611C>T
|
NP_004371.2:p.His871Tyr
|
|
XM_005255124.3:c.2566C>T
|
XP_005255181.1:p.His856Tyr
|
|
XM_005255125.3:c.2464-1486C>T
|
XP_005255182.1:n.2464-1486C>T
|
|
XM_006720848.2:c.2611C>T
|
XP_006720911.1:p.His871Tyr
|
|
XM_011522380.1:c.2557C>T
|
XP_011520682.1:p.His853Tyr
|
|
XM_011522381.1:c.1858C>T
|
XP_011520683.1:p.His620Tyr
|
|
XM_011522382.1:c.2611C>T
|
XP_011520684.1:p.His871Tyr
|
|
XM_005255124.4:c.2566C>T
|
XP_005255181.1:p.His856Tyr
|
|
XM_005255125.4:c.2464-1486C>T
|
XP_005255182.1:n.2464-1486C>T
|
|
XM_006720848.3:c.2611C>T
|
XP_006720911.1:p.His871Tyr
|
|
XM_011522381.2:c.1858C>T
|
XP_011520683.1:p.His620Tyr
|
|
XM_011522382.3:c.2611C>T
|
XP_011520684.1:p.His871Tyr
|
|
XM_017022944.1:c.2605C>T
|
XP_016878433.1:p.His869Tyr
|
|
NM_004380.3:c.2611C>T
MANE Select
|
NP_004371.2:p.His871Tyr
|
|