ENST00000209873.9:c.1462A>G
MANE Select
|
ENSP00000209873.4:p.Asn488Asp
|
|
ENST00000546562.6:n.2526A>G
|
|
|
ENST00000547238.6:n.2098A>G
|
|
|
ENST00000547520.6:n.1578A>G
|
|
|
ENST00000547757.2:c.*380A>G
|
ENSP00000448020.2:n.*380A>G
|
|
ENST00000548880.2:n.1912A>G
|
|
|
ENST00000548931.6:c.897A>G
|
ENSP00000457518.1:p.Ser299=
|
|
ENST00000549450.6:n.1396A>G
|
|
|
ENST00000552161.6:n.2540A>G
|
|
|
ENST00000672797.1:n.1951A>G
|
|
|
ENST00000209873.8:c.1462A>G
|
ENSP00000209873.4:p.Asn488Asp
|
|
ENST00000394384.7:c.1363A>G
|
ENSP00000377908.3:p.Asn455Asp
|
|
ENST00000548931.5:c.897A>G
|
ENSP00000457518.1:p.Ser299=
|
|
ENST00000550286.5:c.1090A>G
|
ENSP00000446885.1:p.Asn364Asp
|
|
ENST00000552876.5:n.1805A>G
|
|
|
NM_001173466.1:c.1363A>G
|
NP_001166937.1:p.Asn455Asp
|
|
NM_015665.5:c.1462A>G
|
NP_056480.1:p.Asn488Asp
|
|
XM_006719617.2:c.1477A>G
|
XP_006719680.1:p.Asn493Asp
|
|
XM_011538777.1:c.1519A>G
|
XP_011537079.1:p.Asn507Asp
|
|
XM_011538778.1:c.1504A>G
|
XP_011537080.1:p.Asn502Asp
|
|
XM_011538779.1:c.1420A>G
|
XP_011537081.1:p.Asn474Asp
|
|
XM_011538780.1:c.1405A>G
|
XP_011537082.1:p.Asn469Asp
|
|
XM_011538781.1:c.853A>G
|
XP_011537083.1:p.Asn285Asp
|
|
XM_011538778.2:c.1504A>G
|
XP_011537080.1:p.Asn502Asp
|
|
XM_011538780.2:c.1405A>G
|
XP_011537082.1:p.Asn469Asp
|
|
XR_001748875.2:n.1519A>G
|
|
|
NM_015665.6:c.1462A>G
MANE Select
|
NP_056480.1:p.Asn488Asp
|
|
NM_001173466.2:c.1363A>G
|
NP_001166937.1:p.Asn455Asp
|
|