ENST00000209873.9:c.1492C>G
MANE Select
|
ENSP00000209873.4:p.Leu498Val
|
|
ENST00000546562.6:n.2556C>G
|
|
|
ENST00000547238.6:n.2128C>G
|
|
|
ENST00000547520.6:n.1608C>G
|
|
|
ENST00000547757.2:c.*410C>G
|
ENSP00000448020.2:n.*410C>G
|
|
ENST00000548931.6:c.927C>G
|
ENSP00000457518.1:p.Cys309Trp
|
|
ENST00000549450.6:n.1426C>G
|
|
|
ENST00000672797.1:n.1981C>G
|
|
|
ENST00000209873.8:c.1492C>G
|
ENSP00000209873.4:p.Leu498Val
|
|
ENST00000394384.7:c.1393C>G
|
ENSP00000377908.3:p.Leu465Val
|
|
ENST00000548931.5:c.927C>G
|
ENSP00000457518.1:p.Cys309Trp
|
|
ENST00000550286.5:c.1120C>G
|
ENSP00000446885.1:p.Leu374Val
|
|
ENST00000552876.5:n.1835C>G
|
|
|
NM_001173466.1:c.1393C>G
|
NP_001166937.1:p.Leu465Val
|
|
NM_015665.5:c.1492C>G
|
NP_056480.1:p.Leu498Val
|
|
XM_006719617.2:c.1507C>G
|
XP_006719680.1:p.Leu503Val
|
|
XM_011538777.1:c.1549C>G
|
XP_011537079.1:p.Leu517Val
|
|
XM_011538778.1:c.1534C>G
|
XP_011537080.1:p.Leu512Val
|
|
XM_011538779.1:c.1450C>G
|
XP_011537081.1:p.Leu484Val
|
|
XM_011538780.1:c.1435C>G
|
XP_011537082.1:p.Leu479Val
|
|
XM_011538781.1:c.883C>G
|
XP_011537083.1:p.Leu295Val
|
|
XM_011538778.2:c.1534C>G
|
XP_011537080.1:p.Leu512Val
|
|
XM_011538780.2:c.1435C>G
|
XP_011537082.1:p.Leu479Val
|
|
XR_001748875.2:n.1549C>G
|
|
|
NM_015665.6:c.1492C>G
MANE Select
|
NP_056480.1:p.Leu498Val
|
|
NM_001173466.2:c.1393C>G
|
NP_001166937.1:p.Leu465Val
|
|