ENST00000209873.9:c.1542C>A
MANE Select
|
ENSP00000209873.4:p.Asp514Glu
|
|
ENST00000546562.6:n.2606C>A
|
|
|
ENST00000547238.6:n.2178C>A
|
|
|
ENST00000547520.6:n.1658C>A
|
|
|
ENST00000547757.2:c.*460C>A
|
ENSP00000448020.2:n.*460C>A
|
|
ENST00000548931.6:c.977C>A
|
ENSP00000457518.1:p.Thr326Asn
|
|
ENST00000549450.6:n.1476C>A
|
|
|
ENST00000672797.1:n.2031C>A
|
|
|
ENST00000209873.8:c.1542C>A
|
ENSP00000209873.4:p.Asp514Glu
|
|
ENST00000394384.7:c.1443C>A
|
ENSP00000377908.3:p.Asp481Glu
|
|
ENST00000548931.5:c.977C>A
|
ENSP00000457518.1:p.Thr326Asn
|
|
ENST00000550286.5:c.1170C>A
|
ENSP00000446885.1:p.Asp390Glu
|
|
ENST00000552876.5:n.1885C>A
|
|
|
NM_001173466.1:c.1443C>A
|
NP_001166937.1:p.Asp481Glu
|
|
NM_015665.5:c.1542C>A
|
NP_056480.1:p.Asp514Glu
|
|
XM_006719617.2:c.1557C>A
|
XP_006719680.1:p.Asp519Glu
|
|
XM_011538777.1:c.1599C>A
|
XP_011537079.1:p.Asp533Glu
|
|
XM_011538778.1:c.1584C>A
|
XP_011537080.1:p.Asp528Glu
|
|
XM_011538779.1:c.1500C>A
|
XP_011537081.1:p.Asp500Glu
|
|
XM_011538780.1:c.1485C>A
|
XP_011537082.1:p.Asp495Glu
|
|
XM_011538781.1:c.933C>A
|
XP_011537083.1:p.Asp311Glu
|
|
XM_011538778.2:c.1584C>A
|
XP_011537080.1:p.Asp528Glu
|
|
XM_011538780.2:c.1485C>A
|
XP_011537082.1:p.Asp495Glu
|
|
XR_001748875.2:n.1599C>A
|
|
|
NM_015665.6:c.1542C>A
MANE Select
|
NP_056480.1:p.Asp514Glu
|
|
NM_001173466.2:c.1443C>A
|
NP_001166937.1:p.Asp481Glu
|
|