ENST00000576892.8:c.581C>T
MANE Select
|
ENSP00000461135.1:p.Ala194Val
|
|
ENST00000429336.5:c.193+1965C>T
|
|
|
ENST00000440428.5:c.581C>T
|
ENSP00000402949.2:p.Ala194Val
|
|
ENST00000576892.7:c.581C>T
|
ENSP00000461135.1:p.Ala194Val
|
|
ENST00000614850.1:c.277+3422C>T
|
|
|
ENST00000614851.4:c.402C>T
|
|
|
ENST00000620088.4:c.*457C>T
|
ENSP00000484108.1:n.*457C>T
|
|
ENST00000621629.4:c.*457C>T
|
ENSP00000478747.1:n.*457C>T
|
|
ENST00000621817.1:c.*746C>T
|
ENSP00000481634.1:n.*746C>T
|
|
NM_001130997.2:c.581C>T
|
NP_001124469.1:p.Ala194Val
|
|
NM_152274.4:c.581C>T
|
NP_689487.2:p.Ala194Val
|
|
XM_005277920.3:c.551C>T
|
XP_005277977.1:p.Ala184Val
|
|
XM_005277921.3:c.551C>T
|
XP_005277978.1:p.Ala184Val
|
|
XM_011531213.1:c.455C>T
|
XP_011529515.1:p.Ala152Val
|
|
XM_011531214.1:c.455C>T
|
XP_011529516.1:p.Ala152Val
|
|
XM_011531215.1:c.455C>T
|
XP_011529517.1:p.Ala152Val
|
|
XM_005277920.4:c.551C>T
|
XP_005277977.1:p.Ala184Val
|
|
XM_005277921.4:c.551C>T
|
XP_005277978.1:p.Ala184Val
|
|
XM_011531214.2:c.455C>T
|
XP_011529516.1:p.Ala152Val
|
|
XM_011531215.2:c.455C>T
|
XP_011529517.1:p.Ala152Val
|
|
XR_002958810.1:n.2486C>T
|
|
|
NM_152274.5:c.581C>T
MANE Select
|
NP_689487.2:p.Ala194Val
|
|
NM_001130997.3:c.581C>T
|
NP_001124469.1:p.Ala194Val
|
|