ENST00000209873.9:c.1620C>G
MANE Select
|
ENSP00000209873.4:p.His540Gln
|
|
ENST00000546562.6:n.2684C>G
|
|
|
ENST00000547757.2:c.*538C>G
|
ENSP00000448020.2:n.*538C>G
|
|
ENST00000548931.6:c.1055C>G
|
ENSP00000457518.1:p.Thr352Ser
|
|
ENST00000549450.6:n.1554C>G
|
|
|
ENST00000209873.8:c.1620C>G
|
ENSP00000209873.4:p.His540Gln
|
|
ENST00000394384.7:c.1521C>G
|
ENSP00000377908.3:p.His507Gln
|
|
ENST00000548931.5:c.1055C>G
|
ENSP00000457518.1:p.Thr352Ser
|
|
ENST00000550286.5:c.1248C>G
|
ENSP00000446885.1:p.His416Gln
|
|
ENST00000552876.5:n.1963C>G
|
|
|
NM_001173466.1:c.1521C>G
|
NP_001166937.1:p.His507Gln
|
|
NM_015665.5:c.1620C>G
|
NP_056480.1:p.His540Gln
|
|
XM_006719617.2:c.1635C>G
|
XP_006719680.1:p.His545Gln
|
|
XM_011538777.1:c.1677C>G
|
XP_011537079.1:p.His559Gln
|
|
XM_011538778.1:c.1662C>G
|
XP_011537080.1:p.His554Gln
|
|
XM_011538779.1:c.1578C>G
|
XP_011537081.1:p.His526Gln
|
|
XM_011538780.1:c.1563C>G
|
XP_011537082.1:p.His521Gln
|
|
XM_011538781.1:c.1011C>G
|
XP_011537083.1:p.His337Gln
|
|
XM_011538778.2:c.1662C>G
|
XP_011537080.1:p.His554Gln
|
|
XM_011538780.2:c.1563C>G
|
XP_011537082.1:p.His521Gln
|
|
XR_001748875.2:n.1677C>G
|
|
|
NM_015665.6:c.1620C>G
MANE Select
|
NP_056480.1:p.His540Gln
|
|
NM_001173466.2:c.1521C>G
|
NP_001166937.1:p.His507Gln
|
|