ENST00000337299.7:c.440G>T
|
ENSP00000338213.6:p.Gly147Val
|
|
ENST00000380518.8:c.647G>T
MANE Select
|
ENSP00000369889.3:p.Gly216Val
|
|
ENST00000337299.6:c.440G>T
|
ENSP00000338213.6:p.Gly147Val
|
|
ENST00000380518.7:c.647G>T
|
ENSP00000369889.3:p.Gly216Val
|
|
NM_001844.4:c.647G>T
|
NP_001835.3:p.Gly216Val
|
|
NM_033150.2:c.440G>T
|
NP_149162.2:p.Gly147Val
|
|
XM_006719242.2:c.791G>T
|
XP_006719305.2:p.Gly264Val
|
|
XM_011537928.1:c.791G>T
|
XP_011536230.1:p.Gly264Val
|
|
XM_011537929.1:c.791G>T
|
XP_011536231.1:p.Gly264Val
|
|
XM_011537930.1:c.791G>T
|
XP_011536232.1:p.Gly264Val
|
|
XM_011537931.1:c.791G>T
|
XP_011536233.1:p.Gly264Val
|
|
XM_011537932.1:c.791G>T
|
XP_011536234.1:p.Gly264Val
|
|
XM_011537933.1:c.791G>T
|
XP_011536235.1:p.Gly264Val
|
|
XM_011537934.1:c.788G>T
|
XP_011536236.1:p.Gly263Val
|
|
XM_017018828.1:c.791G>T
|
XP_016874317.1:p.Gly264Val
|
|
XM_017018829.1:c.788G>T
|
XP_016874318.1:p.Gly263Val
|
|
XM_017018830.1:c.581G>T
|
XP_016874319.1:p.Gly194Val
|
|
XM_017018831.2:c.101G>T
|
XP_016874320.1:p.Gly34Val
|
|
NM_001844.5:c.647G>T
MANE Select
|
NP_001835.3:p.Gly216Val
|
|
NM_033150.3:c.440G>T
|
NP_149162.2:p.Gly147Val
|
|