ENST00000209873.9:c.1493T>A
MANE Select
|
ENSP00000209873.4:p.Leu498His
|
|
ENST00000546562.6:n.2557T>A
|
|
|
ENST00000547238.6:n.2129T>A
|
|
|
ENST00000547520.6:n.1609T>A
|
|
|
ENST00000547757.2:c.*411T>A
|
ENSP00000448020.2:n.*411T>A
|
|
ENST00000548931.6:c.928T>A
|
ENSP00000457518.1:p.Leu310Met
|
|
ENST00000549450.6:n.1427T>A
|
|
|
ENST00000672797.1:n.1982T>A
|
|
|
ENST00000209873.8:c.1493T>A
|
ENSP00000209873.4:p.Leu498His
|
|
ENST00000394384.7:c.1394T>A
|
ENSP00000377908.3:p.Leu465His
|
|
ENST00000548931.5:c.928T>A
|
ENSP00000457518.1:p.Leu310Met
|
|
ENST00000550286.5:c.1121T>A
|
ENSP00000446885.1:p.Leu374His
|
|
ENST00000552876.5:n.1836T>A
|
|
|
NM_001173466.1:c.1394T>A
|
NP_001166937.1:p.Leu465His
|
|
NM_015665.5:c.1493T>A
|
NP_056480.1:p.Leu498His
|
|
XM_006719617.2:c.1508T>A
|
XP_006719680.1:p.Leu503His
|
|
XM_011538777.1:c.1550T>A
|
XP_011537079.1:p.Leu517His
|
|
XM_011538778.1:c.1535T>A
|
XP_011537080.1:p.Leu512His
|
|
XM_011538779.1:c.1451T>A
|
XP_011537081.1:p.Leu484His
|
|
XM_011538780.1:c.1436T>A
|
XP_011537082.1:p.Leu479His
|
|
XM_011538781.1:c.884T>A
|
XP_011537083.1:p.Leu295His
|
|
XM_011538778.2:c.1535T>A
|
XP_011537080.1:p.Leu512His
|
|
XM_011538780.2:c.1436T>A
|
XP_011537082.1:p.Leu479His
|
|
XR_001748875.2:n.1550T>A
|
|
|
NM_015665.6:c.1493T>A
MANE Select
|
NP_056480.1:p.Leu498His
|
|
NM_001173466.2:c.1394T>A
|
NP_001166937.1:p.Leu465His
|
|