ENST00000261304.7:c.1579C>T
MANE Select
|
ENSP00000261304.2:p.His527Tyr
|
|
ENST00000261304.6:c.1579C>T
|
ENSP00000261304.2:p.His527Tyr
|
|
ENST00000393568.8:c.1510C>T
|
ENSP00000377198.4:p.His504Tyr
|
|
ENST00000393569.6:c.1501C>T
|
ENSP00000377199.2:p.His501Tyr
|
|
ENST00000544807.6:c.1411C>T
|
ENSP00000437513.2:p.His471Tyr
|
|
ENST00000555000.5:c.946C>T
|
ENSP00000450472.1:p.His316Tyr
|
|
ENST00000555179.1:c.206+2084C>T
|
|
|
ENST00000557316.5:c.*977C>T
|
ENSP00000452314.1:n.*977C>T
|
|
NM_000153.3:c.1579C>T
|
NP_000144.2:p.His527Tyr
|
|
NM_001201401.1:c.1510C>T
|
NP_001188330.1:p.His504Tyr
|
|
NM_001201402.1:c.1501C>T
|
NP_001188331.1:p.His501Tyr
|
|
XM_011536618.1:c.1411C>T
|
XP_011534920.1:p.His471Tyr
|
|
XM_011536618.2:c.1411C>T
|
XP_011534920.1:p.His471Tyr
|
|
NM_000153.4:c.1579C>T
MANE Select
|
NP_000144.2:p.His527Tyr
|
|
NM_001201401.2:c.1510C>T
|
NP_001188330.1:p.His504Tyr
|
|
NM_001201402.2:c.1501C>T
|
NP_001188331.1:p.His501Tyr
|
|