ENST00000209873.9:c.1464T>A
MANE Select
|
ENSP00000209873.4:p.Asn488Lys
|
|
ENST00000546562.6:n.2528T>A
|
|
|
ENST00000547238.6:n.2100T>A
|
|
|
ENST00000547520.6:n.1580T>A
|
|
|
ENST00000547757.2:c.*382T>A
|
ENSP00000448020.2:n.*382T>A
|
|
ENST00000548880.2:n.1914T>A
|
|
|
ENST00000548931.6:c.899T>A
|
ENSP00000457518.1:p.Met300Lys
|
|
ENST00000549450.6:n.1398T>A
|
|
|
ENST00000552161.6:n.2542T>A
|
|
|
ENST00000672797.1:n.1953T>A
|
|
|
ENST00000209873.8:c.1464T>A
|
ENSP00000209873.4:p.Asn488Lys
|
|
ENST00000394384.7:c.1365T>A
|
ENSP00000377908.3:p.Asn455Lys
|
|
ENST00000548931.5:c.899T>A
|
ENSP00000457518.1:p.Met300Lys
|
|
ENST00000550286.5:c.1092T>A
|
ENSP00000446885.1:p.Asn364Lys
|
|
ENST00000552876.5:n.1807T>A
|
|
|
NM_001173466.1:c.1365T>A
|
NP_001166937.1:p.Asn455Lys
|
|
NM_015665.5:c.1464T>A
|
NP_056480.1:p.Asn488Lys
|
|
XM_006719617.2:c.1479T>A
|
XP_006719680.1:p.Asn493Lys
|
|
XM_011538777.1:c.1521T>A
|
XP_011537079.1:p.Asn507Lys
|
|
XM_011538778.1:c.1506T>A
|
XP_011537080.1:p.Asn502Lys
|
|
XM_011538779.1:c.1422T>A
|
XP_011537081.1:p.Asn474Lys
|
|
XM_011538780.1:c.1407T>A
|
XP_011537082.1:p.Asn469Lys
|
|
XM_011538781.1:c.855T>A
|
XP_011537083.1:p.Asn285Lys
|
|
XM_011538778.2:c.1506T>A
|
XP_011537080.1:p.Asn502Lys
|
|
XM_011538780.2:c.1407T>A
|
XP_011537082.1:p.Asn469Lys
|
|
XR_001748875.2:n.1521T>A
|
|
|
NM_015665.6:c.1464T>A
MANE Select
|
NP_056480.1:p.Asn488Lys
|
|
NM_001173466.2:c.1365T>A
|
NP_001166937.1:p.Asn455Lys
|
|