ENST00000209873.9:c.1420T>A
MANE Select
|
ENSP00000209873.4:p.Trp474Arg
|
|
ENST00000546562.6:n.2484T>A
|
|
|
ENST00000547238.6:n.2056T>A
|
|
|
ENST00000547520.6:n.1536T>A
|
|
|
ENST00000547757.2:c.*338T>A
|
ENSP00000448020.2:n.*338T>A
|
|
ENST00000548880.2:n.1870T>A
|
|
|
ENST00000548931.6:c.855T>A
|
ENSP00000457518.1:p.Ala285=
|
|
ENST00000549450.6:n.1354T>A
|
|
|
ENST00000552161.6:n.2498T>A
|
|
|
ENST00000672797.1:n.1909T>A
|
|
|
ENST00000209873.8:c.1420T>A
|
ENSP00000209873.4:p.Trp474Arg
|
|
ENST00000394384.7:c.1321T>A
|
ENSP00000377908.3:p.Trp441Arg
|
|
ENST00000548931.5:c.855T>A
|
ENSP00000457518.1:p.Ala285=
|
|
ENST00000550286.5:c.1048T>A
|
ENSP00000446885.1:p.Trp350Arg
|
|
ENST00000552876.5:n.1763T>A
|
|
|
NM_001173466.1:c.1321T>A
|
NP_001166937.1:p.Trp441Arg
|
|
NM_015665.5:c.1420T>A
|
NP_056480.1:p.Trp474Arg
|
|
XM_006719617.2:c.1435T>A
|
XP_006719680.1:p.Trp479Arg
|
|
XM_011538777.1:c.1477T>A
|
XP_011537079.1:p.Trp493Arg
|
|
XM_011538778.1:c.1462T>A
|
XP_011537080.1:p.Trp488Arg
|
|
XM_011538779.1:c.1378T>A
|
XP_011537081.1:p.Trp460Arg
|
|
XM_011538780.1:c.1363T>A
|
XP_011537082.1:p.Trp455Arg
|
|
XM_011538781.1:c.811T>A
|
XP_011537083.1:p.Trp271Arg
|
|
XM_011538778.2:c.1462T>A
|
XP_011537080.1:p.Trp488Arg
|
|
XM_011538780.2:c.1363T>A
|
XP_011537082.1:p.Trp455Arg
|
|
XR_001748875.2:n.1477T>A
|
|
|
NM_015665.6:c.1420T>A
MANE Select
|
NP_056480.1:p.Trp474Arg
|
|
NM_001173466.2:c.1321T>A
|
NP_001166937.1:p.Trp441Arg
|
|