ENST00000209873.9:c.1451T>C
MANE Select
|
ENSP00000209873.4:p.Leu484Pro
|
|
ENST00000546562.6:n.2515T>C
|
|
|
ENST00000547238.6:n.2087T>C
|
|
|
ENST00000547520.6:n.1567T>C
|
|
|
ENST00000547757.2:c.*369T>C
|
ENSP00000448020.2:n.*369T>C
|
|
ENST00000548880.2:n.1901T>C
|
|
|
ENST00000548931.6:c.886T>C
|
ENSP00000457518.1:p.Cys296Arg
|
|
ENST00000549450.6:n.1385T>C
|
|
|
ENST00000552161.6:n.2529T>C
|
|
|
ENST00000672797.1:n.1940T>C
|
|
|
ENST00000209873.8:c.1451T>C
|
ENSP00000209873.4:p.Leu484Pro
|
|
ENST00000394384.7:c.1352T>C
|
ENSP00000377908.3:p.Leu451Pro
|
|
ENST00000548931.5:c.886T>C
|
ENSP00000457518.1:p.Cys296Arg
|
|
ENST00000550286.5:c.1079T>C
|
ENSP00000446885.1:p.Leu360Pro
|
|
ENST00000552876.5:n.1794T>C
|
|
|
NM_001173466.1:c.1352T>C
|
NP_001166937.1:p.Leu451Pro
|
|
NM_015665.5:c.1451T>C
|
NP_056480.1:p.Leu484Pro
|
|
XM_006719617.2:c.1466T>C
|
XP_006719680.1:p.Leu489Pro
|
|
XM_011538777.1:c.1508T>C
|
XP_011537079.1:p.Leu503Pro
|
|
XM_011538778.1:c.1493T>C
|
XP_011537080.1:p.Leu498Pro
|
|
XM_011538779.1:c.1409T>C
|
XP_011537081.1:p.Leu470Pro
|
|
XM_011538780.1:c.1394T>C
|
XP_011537082.1:p.Leu465Pro
|
|
XM_011538781.1:c.842T>C
|
XP_011537083.1:p.Leu281Pro
|
|
XM_011538778.2:c.1493T>C
|
XP_011537080.1:p.Leu498Pro
|
|
XM_011538780.2:c.1394T>C
|
XP_011537082.1:p.Leu465Pro
|
|
XR_001748875.2:n.1508T>C
|
|
|
NM_015665.6:c.1451T>C
MANE Select
|
NP_056480.1:p.Leu484Pro
|
|
NM_001173466.2:c.1352T>C
|
NP_001166937.1:p.Leu451Pro
|
|