ENST00000209873.9:c.1627C>T
MANE Select
|
ENSP00000209873.4:p.His543Tyr
|
|
ENST00000547757.2:c.*545C>T
|
ENSP00000448020.2:n.*545C>T
|
|
ENST00000548931.6:c.1062C>T
|
ENSP00000457518.1:p.His354=
|
|
ENST00000549450.6:n.1561C>T
|
|
|
ENST00000209873.8:c.1627C>T
|
ENSP00000209873.4:p.His543Tyr
|
|
ENST00000394384.7:c.1528C>T
|
ENSP00000377908.3:p.His510Tyr
|
|
ENST00000548931.5:c.1062C>T
|
ENSP00000457518.1:p.His354=
|
|
ENST00000550286.5:c.1255C>T
|
ENSP00000446885.1:p.His419Tyr
|
|
ENST00000552876.5:n.1970C>T
|
|
|
NM_001173466.1:c.1528C>T
|
NP_001166937.1:p.His510Tyr
|
|
NM_015665.5:c.1627C>T
|
NP_056480.1:p.His543Tyr
|
|
XM_006719617.2:c.1642C>T
|
XP_006719680.1:p.His548Tyr
|
|
XM_011538777.1:c.1684C>T
|
XP_011537079.1:p.His562Tyr
|
|
XM_011538778.1:c.1669C>T
|
XP_011537080.1:p.His557Tyr
|
|
XM_011538779.1:c.1585C>T
|
XP_011537081.1:p.His529Tyr
|
|
XM_011538780.1:c.1570C>T
|
XP_011537082.1:p.His524Tyr
|
|
XM_011538781.1:c.1018C>T
|
XP_011537083.1:p.His340Tyr
|
|
XM_011538778.2:c.1669C>T
|
XP_011537080.1:p.His557Tyr
|
|
XM_011538780.2:c.1570C>T
|
XP_011537082.1:p.His524Tyr
|
|
XR_001748875.2:n.1684C>T
|
|
|
NM_015665.6:c.1627C>T
MANE Select
|
NP_056480.1:p.His543Tyr
|
|
NM_001173466.2:c.1528C>T
|
NP_001166937.1:p.His510Tyr
|
|