ENST00000209873.9:c.1300C>T
MANE Select
|
ENSP00000209873.4:p.Arg434Ter
|
|
ENST00000546562.6:n.2364C>T
|
|
|
ENST00000547238.6:n.1936C>T
|
|
|
ENST00000547520.6:n.1294C>T
|
|
|
ENST00000547757.2:c.349C>T
|
ENSP00000448020.2:p.Arg117Ter
|
|
ENST00000548880.2:n.1750C>T
|
|
|
ENST00000548931.6:c.820C>T
|
ENSP00000457518.1:p.Arg274Ter
|
|
ENST00000549450.6:n.1234C>T
|
|
|
ENST00000552161.6:n.2256C>T
|
|
|
ENST00000672797.1:n.1789C>T
|
|
|
ENST00000672900.1:n.2390C>T
|
|
|
ENST00000209873.8:c.1300C>T
|
ENSP00000209873.4:p.Arg434Ter
|
|
ENST00000394384.7:c.1201C>T
|
ENSP00000377908.3:p.Arg401Ter
|
|
ENST00000548931.5:c.820C>T
|
ENSP00000457518.1:p.Arg274Ter
|
|
ENST00000550033.5:n.555C>T
|
|
|
ENST00000550286.5:c.928C>T
|
ENSP00000446885.1:p.Arg310Ter
|
|
ENST00000552876.5:n.1643C>T
|
|
|
NM_001173466.1:c.1201C>T
|
NP_001166937.1:p.Arg401Ter
|
|
NM_015665.5:c.1300C>T
|
NP_056480.1:p.Arg434Ter
|
|
XM_006719617.2:c.1315C>T
|
XP_006719680.1:p.Arg439Ter
|
|
XM_011538777.1:c.1315C>T
|
XP_011537079.1:p.Arg439Ter
|
|
XM_011538778.1:c.1300C>T
|
XP_011537080.1:p.Arg434Ter
|
|
XM_011538779.1:c.1216C>T
|
XP_011537081.1:p.Arg406Ter
|
|
XM_011538780.1:c.1201C>T
|
XP_011537082.1:p.Arg401Ter
|
|
XM_011538781.1:c.649C>T
|
XP_011537083.1:p.Arg217Ter
|
|
XM_011538778.2:c.1300C>T
|
XP_011537080.1:p.Arg434Ter
|
|
XM_011538780.2:c.1201C>T
|
XP_011537082.1:p.Arg401Ter
|
|
XR_001748875.2:n.1357C>T
|
|
|
NM_015665.6:c.1300C>T
MANE Select
|
NP_056480.1:p.Arg434Ter
|
|
NM_001173466.2:c.1201C>T
|
NP_001166937.1:p.Arg401Ter
|
|