ENST00000209873.9:c.1551C>T
MANE Select
|
ENSP00000209873.4:p.Leu517=
|
|
ENST00000546562.6:n.2615C>T
|
|
|
ENST00000547238.6:n.2187C>T
|
|
|
ENST00000547520.6:n.1667C>T
|
|
|
ENST00000547757.2:c.*469C>T
|
ENSP00000448020.2:n.*469C>T
|
|
ENST00000548931.6:c.986C>T
|
ENSP00000457518.1:p.Ser329Phe
|
|
ENST00000549450.6:n.1485C>T
|
|
|
ENST00000672797.1:n.2040C>T
|
|
|
ENST00000209873.8:c.1551C>T
|
ENSP00000209873.4:p.Leu517=
|
|
ENST00000394384.7:c.1452C>T
|
ENSP00000377908.3:p.Leu484=
|
|
ENST00000548931.5:c.986C>T
|
ENSP00000457518.1:p.Ser329Phe
|
|
ENST00000550286.5:c.1179C>T
|
ENSP00000446885.1:p.Leu393=
|
|
ENST00000552876.5:n.1894C>T
|
|
|
NM_001173466.1:c.1452C>T
|
NP_001166937.1:p.Leu484=
|
|
NM_015665.5:c.1551C>T
|
NP_056480.1:p.Leu517=
|
|
XM_006719617.2:c.1566C>T
|
XP_006719680.1:p.Leu522=
|
|
XM_011538777.1:c.1608C>T
|
XP_011537079.1:p.Leu536=
|
|
XM_011538778.1:c.1593C>T
|
XP_011537080.1:p.Leu531=
|
|
XM_011538779.1:c.1509C>T
|
XP_011537081.1:p.Leu503=
|
|
XM_011538780.1:c.1494C>T
|
XP_011537082.1:p.Leu498=
|
|
XM_011538781.1:c.942C>T
|
XP_011537083.1:p.Leu314=
|
|
XM_011538778.2:c.1593C>T
|
XP_011537080.1:p.Leu531=
|
|
XM_011538780.2:c.1494C>T
|
XP_011537082.1:p.Leu498=
|
|
XR_001748875.2:n.1608C>T
|
|
|
NM_015665.6:c.1551C>T
MANE Select
|
NP_056480.1:p.Leu517=
|
|
NM_001173466.2:c.1452C>T
|
NP_001166937.1:p.Leu484=
|
|