ENST00000209873.9:c.1633C>G
MANE Select
|
ENSP00000209873.4:p.His545Asp
|
|
ENST00000547757.2:c.*551C>G
|
ENSP00000448020.2:n.*551C>G
|
|
ENST00000548931.6:c.1068C>G
|
ENSP00000457518.1:p.Pro356=
|
|
ENST00000549450.6:n.1567C>G
|
|
|
ENST00000209873.8:c.1633C>G
|
ENSP00000209873.4:p.His545Asp
|
|
ENST00000394384.7:c.1534C>G
|
ENSP00000377908.3:p.His512Asp
|
|
ENST00000548931.5:c.1068C>G
|
ENSP00000457518.1:p.Pro356=
|
|
ENST00000550286.5:c.1261C>G
|
ENSP00000446885.1:p.His421Asp
|
|
ENST00000552876.5:n.1976C>G
|
|
|
NM_001173466.1:c.1534C>G
|
NP_001166937.1:p.His512Asp
|
|
NM_015665.5:c.1633C>G
|
NP_056480.1:p.His545Asp
|
|
XM_006719617.2:c.1648C>G
|
XP_006719680.1:p.His550Asp
|
|
XM_011538777.1:c.1690C>G
|
XP_011537079.1:p.His564Asp
|
|
XM_011538778.1:c.1675C>G
|
XP_011537080.1:p.His559Asp
|
|
XM_011538779.1:c.1591C>G
|
XP_011537081.1:p.His531Asp
|
|
XM_011538780.1:c.1576C>G
|
XP_011537082.1:p.His526Asp
|
|
XM_011538781.1:c.1024C>G
|
XP_011537083.1:p.His342Asp
|
|
XM_011538778.2:c.1675C>G
|
XP_011537080.1:p.His559Asp
|
|
XM_011538780.2:c.1576C>G
|
XP_011537082.1:p.His526Asp
|
|
XR_001748875.2:n.1690C>G
|
|
|
NM_015665.6:c.1633C>G
MANE Select
|
NP_056480.1:p.His545Asp
|
|
NM_001173466.2:c.1534C>G
|
NP_001166937.1:p.His512Asp
|
|