ENST00000209873.9:c.1445T>C
MANE Select
|
ENSP00000209873.4:p.Ile482Thr
|
|
ENST00000546562.6:n.2509T>C
|
|
|
ENST00000547238.6:n.2081T>C
|
|
|
ENST00000547520.6:n.1561T>C
|
|
|
ENST00000547757.2:c.*363T>C
|
ENSP00000448020.2:n.*363T>C
|
|
ENST00000548880.2:n.1895T>C
|
|
|
ENST00000548931.6:c.880T>C
|
ENSP00000457518.1:p.Ser294Pro
|
|
ENST00000549450.6:n.1379T>C
|
|
|
ENST00000552161.6:n.2523T>C
|
|
|
ENST00000672797.1:n.1934T>C
|
|
|
ENST00000209873.8:c.1445T>C
|
ENSP00000209873.4:p.Ile482Thr
|
|
ENST00000394384.7:c.1346T>C
|
ENSP00000377908.3:p.Ile449Thr
|
|
ENST00000548931.5:c.880T>C
|
ENSP00000457518.1:p.Ser294Pro
|
|
ENST00000550286.5:c.1073T>C
|
ENSP00000446885.1:p.Ile358Thr
|
|
ENST00000552876.5:n.1788T>C
|
|
|
NM_001173466.1:c.1346T>C
|
NP_001166937.1:p.Ile449Thr
|
|
NM_015665.5:c.1445T>C
|
NP_056480.1:p.Ile482Thr
|
|
XM_006719617.2:c.1460T>C
|
XP_006719680.1:p.Ile487Thr
|
|
XM_011538777.1:c.1502T>C
|
XP_011537079.1:p.Ile501Thr
|
|
XM_011538778.1:c.1487T>C
|
XP_011537080.1:p.Ile496Thr
|
|
XM_011538779.1:c.1403T>C
|
XP_011537081.1:p.Ile468Thr
|
|
XM_011538780.1:c.1388T>C
|
XP_011537082.1:p.Ile463Thr
|
|
XM_011538781.1:c.836T>C
|
XP_011537083.1:p.Ile279Thr
|
|
XM_011538778.2:c.1487T>C
|
XP_011537080.1:p.Ile496Thr
|
|
XM_011538780.2:c.1388T>C
|
XP_011537082.1:p.Ile463Thr
|
|
XR_001748875.2:n.1502T>C
|
|
|
NM_015665.6:c.1445T>C
MANE Select
|
NP_056480.1:p.Ile482Thr
|
|
NM_001173466.2:c.1346T>C
|
NP_001166937.1:p.Ile449Thr
|
|