ENST00000209873.9:c.1618C>T
MANE Select
|
ENSP00000209873.4:p.His540Tyr
|
|
ENST00000546562.6:n.2682C>T
|
|
|
ENST00000547757.2:c.*536C>T
|
ENSP00000448020.2:n.*536C>T
|
|
ENST00000548931.6:c.1053C>T
|
ENSP00000457518.1:p.Pro351=
|
|
ENST00000549450.6:n.1552C>T
|
|
|
ENST00000209873.8:c.1618C>T
|
ENSP00000209873.4:p.His540Tyr
|
|
ENST00000394384.7:c.1519C>T
|
ENSP00000377908.3:p.His507Tyr
|
|
ENST00000548931.5:c.1053C>T
|
ENSP00000457518.1:p.Pro351=
|
|
ENST00000550286.5:c.1246C>T
|
ENSP00000446885.1:p.His416Tyr
|
|
ENST00000552876.5:n.1961C>T
|
|
|
NM_001173466.1:c.1519C>T
|
NP_001166937.1:p.His507Tyr
|
|
NM_015665.5:c.1618C>T
|
NP_056480.1:p.His540Tyr
|
|
XM_006719617.2:c.1633C>T
|
XP_006719680.1:p.His545Tyr
|
|
XM_011538777.1:c.1675C>T
|
XP_011537079.1:p.His559Tyr
|
|
XM_011538778.1:c.1660C>T
|
XP_011537080.1:p.His554Tyr
|
|
XM_011538779.1:c.1576C>T
|
XP_011537081.1:p.His526Tyr
|
|
XM_011538780.1:c.1561C>T
|
XP_011537082.1:p.His521Tyr
|
|
XM_011538781.1:c.1009C>T
|
XP_011537083.1:p.His337Tyr
|
|
XM_011538778.2:c.1660C>T
|
XP_011537080.1:p.His554Tyr
|
|
XM_011538780.2:c.1561C>T
|
XP_011537082.1:p.His521Tyr
|
|
XR_001748875.2:n.1675C>T
|
|
|
NM_015665.6:c.1618C>T
MANE Select
|
NP_056480.1:p.His540Tyr
|
|
NM_001173466.2:c.1519C>T
|
NP_001166937.1:p.His507Tyr
|
|