ENST00000209873.9:c.1535T>A
MANE Select
|
ENSP00000209873.4:p.Ile512Asn
|
|
ENST00000546562.6:n.2599T>A
|
|
|
ENST00000547238.6:n.2171T>A
|
|
|
ENST00000547520.6:n.1651T>A
|
|
|
ENST00000547757.2:c.*453T>A
|
ENSP00000448020.2:n.*453T>A
|
|
ENST00000548931.6:c.970T>A
|
ENSP00000457518.1:p.Phe324Ile
|
|
ENST00000549450.6:n.1469T>A
|
|
|
ENST00000672797.1:n.2024T>A
|
|
|
ENST00000209873.8:c.1535T>A
|
ENSP00000209873.4:p.Ile512Asn
|
|
ENST00000394384.7:c.1436T>A
|
ENSP00000377908.3:p.Ile479Asn
|
|
ENST00000548931.5:c.970T>A
|
ENSP00000457518.1:p.Phe324Ile
|
|
ENST00000550286.5:c.1163T>A
|
ENSP00000446885.1:p.Ile388Asn
|
|
ENST00000552876.5:n.1878T>A
|
|
|
NM_001173466.1:c.1436T>A
|
NP_001166937.1:p.Ile479Asn
|
|
NM_015665.5:c.1535T>A
|
NP_056480.1:p.Ile512Asn
|
|
XM_006719617.2:c.1550T>A
|
XP_006719680.1:p.Ile517Asn
|
|
XM_011538777.1:c.1592T>A
|
XP_011537079.1:p.Ile531Asn
|
|
XM_011538778.1:c.1577T>A
|
XP_011537080.1:p.Ile526Asn
|
|
XM_011538779.1:c.1493T>A
|
XP_011537081.1:p.Ile498Asn
|
|
XM_011538780.1:c.1478T>A
|
XP_011537082.1:p.Ile493Asn
|
|
XM_011538781.1:c.926T>A
|
XP_011537083.1:p.Ile309Asn
|
|
XM_011538778.2:c.1577T>A
|
XP_011537080.1:p.Ile526Asn
|
|
XM_011538780.2:c.1478T>A
|
XP_011537082.1:p.Ile493Asn
|
|
XR_001748875.2:n.1592T>A
|
|
|
NM_015665.6:c.1535T>A
MANE Select
|
NP_056480.1:p.Ile512Asn
|
|
NM_001173466.2:c.1436T>A
|
NP_001166937.1:p.Ile479Asn
|
|