ENST00000337299.7:c.2978G>T
|
ENSP00000338213.6:p.Gly993Val
|
|
ENST00000380518.8:c.3185G>T
MANE Select
|
ENSP00000369889.3:p.Gly1062Val
|
|
ENST00000337299.6:c.2978G>T
|
ENSP00000338213.6:p.Gly993Val
|
|
ENST00000380518.7:c.3185G>T
|
ENSP00000369889.3:p.Gly1062Val
|
|
ENST00000493991.5:n.2271G>T
|
|
|
ENST00000546974.1:n.38G>T
|
|
|
NM_001844.4:c.3185G>T
|
NP_001835.3:p.Gly1062Val
|
|
NM_033150.2:c.2978G>T
|
NP_149162.2:p.Gly993Val
|
|
XM_006719242.2:c.3329G>T
|
XP_006719305.2:p.Gly1110Val
|
|
XM_011537928.1:c.3329G>T
|
XP_011536230.1:p.Gly1110Val
|
|
XM_011537929.1:c.3329G>T
|
XP_011536231.1:p.Gly1110Val
|
|
XM_011537930.1:c.3329G>T
|
XP_011536232.1:p.Gly1110Val
|
|
XM_011537931.1:c.3329G>T
|
XP_011536233.1:p.Gly1110Val
|
|
XM_011537932.1:c.3329G>T
|
XP_011536234.1:p.Gly1110Val
|
|
XM_011537933.1:c.3329G>T
|
XP_011536235.1:p.Gly1110Val
|
|
XM_011537934.1:c.3326G>T
|
XP_011536236.1:p.Gly1109Val
|
|
XM_011537935.1:c.2273G>T
|
XP_011536237.1:p.Gly758Val
|
|
XM_017018828.1:c.3329G>T
|
XP_016874317.1:p.Gly1110Val
|
|
XM_017018829.1:c.3326G>T
|
XP_016874318.1:p.Gly1109Val
|
|
XM_017018830.1:c.3119G>T
|
XP_016874319.1:p.Gly1040Val
|
|
XM_017018831.2:c.2639G>T
|
XP_016874320.1:p.Gly880Val
|
|
NM_001844.5:c.3185G>T
MANE Select
|
NP_001835.3:p.Gly1062Val
|
|
NM_033150.3:c.2978G>T
|
NP_149162.2:p.Gly993Val
|
|