ENST00000337299.7:c.1424C>T
|
ENSP00000338213.6:p.Ala475Val
|
|
ENST00000380518.8:c.1631C>T
MANE Select
|
ENSP00000369889.3:p.Ala544Val
|
|
ENST00000337299.6:c.1424C>T
|
ENSP00000338213.6:p.Ala475Val
|
|
ENST00000380518.7:c.1631C>T
|
ENSP00000369889.3:p.Ala544Val
|
|
ENST00000493991.5:n.555C>T
|
|
|
NM_001844.4:c.1631C>T
|
NP_001835.3:p.Ala544Val
|
|
NM_033150.2:c.1424C>T
|
NP_149162.2:p.Ala475Val
|
|
XM_006719242.2:c.1775C>T
|
XP_006719305.2:p.Ala592Val
|
|
XM_011537928.1:c.1775C>T
|
XP_011536230.1:p.Ala592Val
|
|
XM_011537929.1:c.1775C>T
|
XP_011536231.1:p.Ala592Val
|
|
XM_011537930.1:c.1775C>T
|
XP_011536232.1:p.Ala592Val
|
|
XM_011537931.1:c.1775C>T
|
XP_011536233.1:p.Ala592Val
|
|
XM_011537932.1:c.1775C>T
|
XP_011536234.1:p.Ala592Val
|
|
XM_011537933.1:c.1775C>T
|
XP_011536235.1:p.Ala592Val
|
|
XM_011537934.1:c.1772C>T
|
XP_011536236.1:p.Ala591Val
|
|
XM_011537935.1:c.719C>T
|
XP_011536237.1:p.Ala240Val
|
|
XM_017018828.1:c.1775C>T
|
XP_016874317.1:p.Ala592Val
|
|
XM_017018829.1:c.1772C>T
|
XP_016874318.1:p.Ala591Val
|
|
XM_017018830.1:c.1565C>T
|
XP_016874319.1:p.Ala522Val
|
|
XM_017018831.2:c.1085C>T
|
XP_016874320.1:p.Ala362Val
|
|
NM_001844.5:c.1631C>T
MANE Select
|
NP_001835.3:p.Ala544Val
|
|
NM_033150.3:c.1424C>T
|
NP_149162.2:p.Ala475Val
|
|