ENST00000209873.9:c.1435A>T
MANE Select
|
ENSP00000209873.4:p.Ile479Phe
|
|
ENST00000546562.6:n.2499A>T
|
|
|
ENST00000547238.6:n.2071A>T
|
|
|
ENST00000547520.6:n.1551A>T
|
|
|
ENST00000547757.2:c.*353A>T
|
ENSP00000448020.2:n.*353A>T
|
|
ENST00000548880.2:n.1885A>T
|
|
|
ENST00000548931.6:c.870A>T
|
ENSP00000457518.1:p.Glu290Asp
|
|
ENST00000549450.6:n.1369A>T
|
|
|
ENST00000552161.6:n.2513A>T
|
|
|
ENST00000672797.1:n.1924A>T
|
|
|
ENST00000209873.8:c.1435A>T
|
ENSP00000209873.4:p.Ile479Phe
|
|
ENST00000394384.7:c.1336A>T
|
ENSP00000377908.3:p.Ile446Phe
|
|
ENST00000548931.5:c.870A>T
|
ENSP00000457518.1:p.Glu290Asp
|
|
ENST00000550286.5:c.1063A>T
|
ENSP00000446885.1:p.Ile355Phe
|
|
ENST00000552876.5:n.1778A>T
|
|
|
NM_001173466.1:c.1336A>T
|
NP_001166937.1:p.Ile446Phe
|
|
NM_015665.5:c.1435A>T
|
NP_056480.1:p.Ile479Phe
|
|
XM_006719617.2:c.1450A>T
|
XP_006719680.1:p.Ile484Phe
|
|
XM_011538777.1:c.1492A>T
|
XP_011537079.1:p.Ile498Phe
|
|
XM_011538778.1:c.1477A>T
|
XP_011537080.1:p.Ile493Phe
|
|
XM_011538779.1:c.1393A>T
|
XP_011537081.1:p.Ile465Phe
|
|
XM_011538780.1:c.1378A>T
|
XP_011537082.1:p.Ile460Phe
|
|
XM_011538781.1:c.826A>T
|
XP_011537083.1:p.Ile276Phe
|
|
XM_011538778.2:c.1477A>T
|
XP_011537080.1:p.Ile493Phe
|
|
XM_011538780.2:c.1378A>T
|
XP_011537082.1:p.Ile460Phe
|
|
XR_001748875.2:n.1492A>T
|
|
|
NM_015665.6:c.1435A>T
MANE Select
|
NP_056480.1:p.Ile479Phe
|
|
NM_001173466.2:c.1336A>T
|
NP_001166937.1:p.Ile446Phe
|
|