ENST00000209873.9:c.1460T>A
MANE Select
|
ENSP00000209873.4:p.Val487Asp
|
|
ENST00000546562.6:n.2524T>A
|
|
|
ENST00000547238.6:n.2096T>A
|
|
|
ENST00000547520.6:n.1576T>A
|
|
|
ENST00000547757.2:c.*378T>A
|
ENSP00000448020.2:n.*378T>A
|
|
ENST00000548880.2:n.1910T>A
|
|
|
ENST00000548931.6:c.895T>A
|
ENSP00000457518.1:p.Ser299Thr
|
|
ENST00000549450.6:n.1394T>A
|
|
|
ENST00000552161.6:n.2538T>A
|
|
|
ENST00000672797.1:n.1949T>A
|
|
|
ENST00000209873.8:c.1460T>A
|
ENSP00000209873.4:p.Val487Asp
|
|
ENST00000394384.7:c.1361T>A
|
ENSP00000377908.3:p.Val454Asp
|
|
ENST00000548931.5:c.895T>A
|
ENSP00000457518.1:p.Ser299Thr
|
|
ENST00000550286.5:c.1088T>A
|
ENSP00000446885.1:p.Val363Asp
|
|
ENST00000552876.5:n.1803T>A
|
|
|
NM_001173466.1:c.1361T>A
|
NP_001166937.1:p.Val454Asp
|
|
NM_015665.5:c.1460T>A
|
NP_056480.1:p.Val487Asp
|
|
XM_006719617.2:c.1475T>A
|
XP_006719680.1:p.Val492Asp
|
|
XM_011538777.1:c.1517T>A
|
XP_011537079.1:p.Val506Asp
|
|
XM_011538778.1:c.1502T>A
|
XP_011537080.1:p.Val501Asp
|
|
XM_011538779.1:c.1418T>A
|
XP_011537081.1:p.Val473Asp
|
|
XM_011538780.1:c.1403T>A
|
XP_011537082.1:p.Val468Asp
|
|
XM_011538781.1:c.851T>A
|
XP_011537083.1:p.Val284Asp
|
|
XM_011538778.2:c.1502T>A
|
XP_011537080.1:p.Val501Asp
|
|
XM_011538780.2:c.1403T>A
|
XP_011537082.1:p.Val468Asp
|
|
XR_001748875.2:n.1517T>A
|
|
|
NM_015665.6:c.1460T>A
MANE Select
|
NP_056480.1:p.Val487Asp
|
|
NM_001173466.2:c.1361T>A
|
NP_001166937.1:p.Val454Asp
|
|