ENST00000209873.9:c.1539T>A
MANE Select
|
ENSP00000209873.4:p.His513Gln
|
|
ENST00000546562.6:n.2603T>A
|
|
|
ENST00000547238.6:n.2175T>A
|
|
|
ENST00000547520.6:n.1655T>A
|
|
|
ENST00000547757.2:c.*457T>A
|
ENSP00000448020.2:n.*457T>A
|
|
ENST00000548931.6:c.974T>A
|
ENSP00000457518.1:p.Met325Lys
|
|
ENST00000549450.6:n.1473T>A
|
|
|
ENST00000672797.1:n.2028T>A
|
|
|
ENST00000209873.8:c.1539T>A
|
ENSP00000209873.4:p.His513Gln
|
|
ENST00000394384.7:c.1440T>A
|
ENSP00000377908.3:p.His480Gln
|
|
ENST00000548931.5:c.974T>A
|
ENSP00000457518.1:p.Met325Lys
|
|
ENST00000550286.5:c.1167T>A
|
ENSP00000446885.1:p.His389Gln
|
|
ENST00000552876.5:n.1882T>A
|
|
|
NM_001173466.1:c.1440T>A
|
NP_001166937.1:p.His480Gln
|
|
NM_015665.5:c.1539T>A
|
NP_056480.1:p.His513Gln
|
|
XM_006719617.2:c.1554T>A
|
XP_006719680.1:p.His518Gln
|
|
XM_011538777.1:c.1596T>A
|
XP_011537079.1:p.His532Gln
|
|
XM_011538778.1:c.1581T>A
|
XP_011537080.1:p.His527Gln
|
|
XM_011538779.1:c.1497T>A
|
XP_011537081.1:p.His499Gln
|
|
XM_011538780.1:c.1482T>A
|
XP_011537082.1:p.His494Gln
|
|
XM_011538781.1:c.930T>A
|
XP_011537083.1:p.His310Gln
|
|
XM_011538778.2:c.1581T>A
|
XP_011537080.1:p.His527Gln
|
|
XM_011538780.2:c.1482T>A
|
XP_011537082.1:p.His494Gln
|
|
XR_001748875.2:n.1596T>A
|
|
|
NM_015665.6:c.1539T>A
MANE Select
|
NP_056480.1:p.His513Gln
|
|
NM_001173466.2:c.1440T>A
|
NP_001166937.1:p.His480Gln
|
|