ENST00000209873.9:c.1637T>A
MANE Select
|
ENSP00000209873.4:p.Leu546His
|
|
ENST00000547757.2:c.*555T>A
|
ENSP00000448020.2:n.*555T>A
|
|
ENST00000548931.6:c.1072T>A
|
ENSP00000457518.1:p.Ser358Thr
|
|
ENST00000549450.6:n.1571T>A
|
|
|
ENST00000209873.8:c.1637T>A
|
ENSP00000209873.4:p.Leu546His
|
|
ENST00000394384.7:c.1538T>A
|
ENSP00000377908.3:p.Leu513His
|
|
ENST00000548931.5:c.1072T>A
|
ENSP00000457518.1:p.Ser358Thr
|
|
ENST00000550286.5:c.1265T>A
|
ENSP00000446885.1:p.Leu422His
|
|
ENST00000552876.5:n.1980T>A
|
|
|
NM_001173466.1:c.1538T>A
|
NP_001166937.1:p.Leu513His
|
|
NM_015665.5:c.1637T>A
|
NP_056480.1:p.Leu546His
|
|
XM_006719617.2:c.1652T>A
|
XP_006719680.1:p.Leu551His
|
|
XM_011538777.1:c.1694T>A
|
XP_011537079.1:p.Leu565His
|
|
XM_011538778.1:c.1679T>A
|
XP_011537080.1:p.Leu560His
|
|
XM_011538779.1:c.1595T>A
|
XP_011537081.1:p.Leu532His
|
|
XM_011538780.1:c.1580T>A
|
XP_011537082.1:p.Leu527His
|
|
XM_011538781.1:c.1028T>A
|
XP_011537083.1:p.Leu343His
|
|
XM_011538778.2:c.1679T>A
|
XP_011537080.1:p.Leu560His
|
|
XM_011538780.2:c.1580T>A
|
XP_011537082.1:p.Leu527His
|
|
XR_001748875.2:n.1694T>A
|
|
|
NM_015665.6:c.1637T>A
MANE Select
|
NP_056480.1:p.Leu546His
|
|
NM_001173466.2:c.1538T>A
|
NP_001166937.1:p.Leu513His
|
|