ENST00000209873.9:c.1433G>C
MANE Select
|
ENSP00000209873.4:p.Arg478Pro
|
|
ENST00000546562.6:n.2497G>C
|
|
|
ENST00000547238.6:n.2069G>C
|
|
|
ENST00000547520.6:n.1549G>C
|
|
|
ENST00000547757.2:c.*351G>C
|
ENSP00000448020.2:n.*351G>C
|
|
ENST00000548880.2:n.1883G>C
|
|
|
ENST00000548931.6:c.868G>C
|
ENSP00000457518.1:p.Glu290Gln
|
|
ENST00000549450.6:n.1367G>C
|
|
|
ENST00000552161.6:n.2511G>C
|
|
|
ENST00000672797.1:n.1922G>C
|
|
|
ENST00000209873.8:c.1433G>C
|
ENSP00000209873.4:p.Arg478Pro
|
|
ENST00000394384.7:c.1334G>C
|
ENSP00000377908.3:p.Arg445Pro
|
|
ENST00000548931.5:c.868G>C
|
ENSP00000457518.1:p.Glu290Gln
|
|
ENST00000550286.5:c.1061G>C
|
ENSP00000446885.1:p.Arg354Pro
|
|
ENST00000552876.5:n.1776G>C
|
|
|
NM_001173466.1:c.1334G>C
|
NP_001166937.1:p.Arg445Pro
|
|
NM_015665.5:c.1433G>C
|
NP_056480.1:p.Arg478Pro
|
|
XM_006719617.2:c.1448G>C
|
XP_006719680.1:p.Arg483Pro
|
|
XM_011538777.1:c.1490G>C
|
XP_011537079.1:p.Arg497Pro
|
|
XM_011538778.1:c.1475G>C
|
XP_011537080.1:p.Arg492Pro
|
|
XM_011538779.1:c.1391G>C
|
XP_011537081.1:p.Arg464Pro
|
|
XM_011538780.1:c.1376G>C
|
XP_011537082.1:p.Arg459Pro
|
|
XM_011538781.1:c.824G>C
|
XP_011537083.1:p.Arg275Pro
|
|
XM_011538778.2:c.1475G>C
|
XP_011537080.1:p.Arg492Pro
|
|
XM_011538780.2:c.1376G>C
|
XP_011537082.1:p.Arg459Pro
|
|
XR_001748875.2:n.1490G>C
|
|
|
NM_015665.6:c.1433G>C
MANE Select
|
NP_056480.1:p.Arg478Pro
|
|
NM_001173466.2:c.1334G>C
|
NP_001166937.1:p.Arg445Pro
|
|