ENST00000209873.9:c.1058T>C
MANE Select
|
ENSP00000209873.4:p.Ile353Thr
|
|
ENST00000546562.6:n.2122T>C
|
|
|
ENST00000547238.6:n.1694T>C
|
|
|
ENST00000547520.6:n.1052T>C
|
|
|
ENST00000547757.2:c.107T>C
|
ENSP00000448020.2:p.Ile36Thr
|
|
ENST00000548880.2:n.1508T>C
|
|
|
ENST00000548931.6:c.578T>C
|
ENSP00000457518.1:p.Ile193Thr
|
|
ENST00000549450.6:n.992T>C
|
|
|
ENST00000552161.6:n.2014T>C
|
|
|
ENST00000672797.1:n.1547T>C
|
|
|
ENST00000672900.1:n.2000T>C
|
|
|
ENST00000209873.8:c.1058T>C
|
ENSP00000209873.4:p.Ile353Thr
|
|
ENST00000394384.7:c.959T>C
|
ENSP00000377908.3:p.Ile320Thr
|
|
ENST00000547520.5:n.762T>C
|
|
|
ENST00000548931.5:c.578T>C
|
ENSP00000457518.1:p.Ile193Thr
|
|
ENST00000550033.5:n.313T>C
|
|
|
ENST00000550286.5:c.686T>C
|
ENSP00000446885.1:p.Ile229Thr
|
|
ENST00000552876.5:n.1401T>C
|
|
|
NM_001173466.1:c.959T>C
|
NP_001166937.1:p.Ile320Thr
|
|
NM_015665.5:c.1058T>C
|
NP_056480.1:p.Ile353Thr
|
|
XM_006719617.2:c.1073T>C
|
XP_006719680.1:p.Ile358Thr
|
|
XM_011538777.1:c.1073T>C
|
XP_011537079.1:p.Ile358Thr
|
|
XM_011538778.1:c.1058T>C
|
XP_011537080.1:p.Ile353Thr
|
|
XM_011538779.1:c.974T>C
|
XP_011537081.1:p.Ile325Thr
|
|
XM_011538780.1:c.959T>C
|
XP_011537082.1:p.Ile320Thr
|
|
XM_011538781.1:c.407T>C
|
XP_011537083.1:p.Ile136Thr
|
|
XM_011538778.2:c.1058T>C
|
XP_011537080.1:p.Ile353Thr
|
|
XM_011538780.2:c.959T>C
|
XP_011537082.1:p.Ile320Thr
|
|
XR_001748875.2:n.1115T>C
|
|
|
NM_015665.6:c.1058T>C
MANE Select
|
NP_056480.1:p.Ile353Thr
|
|
NM_001173466.2:c.959T>C
|
NP_001166937.1:p.Ile320Thr
|
|