ENST00000264093.9:c.763G>T
(DGUOK)
MANE Select
|
ENSP00000264093.4:p.Asp255Tyr
|
|
ENST00000264093.8:c.763G>T
(DGUOK)
|
ENSP00000264093.4:p.Asp255Tyr
|
|
ENST00000348222.3:c.499G>T
(DGUOK)
|
ENSP00000306964.3:p.Asp167Tyr
|
|
ENST00000418996.5:c.*116G>T
(DGUOK)
|
ENSP00000408209.1:n.*116G>T
|
|
ENST00000462685.1:n.592G>T
(DGUOK)
|
|
|
ENST00000489796.5:n.648G>T
(DGUOK)
|
|
|
ENST00000629438.2:c.*380G>T
(DGUOK)
|
ENSP00000487122.1:n.*380G>T
|
|
NM_080916.2:c.763G>T
(DGUOK)
|
NP_550438.1:p.Asp255Tyr
|
|
NM_080918.2:c.499G>T
(DGUOK)
|
NP_550440.1:p.Asp167Tyr
|
|
NR_104029.1:n.338C>A
(DGUOK-AS1)
|
|
|
NR_104030.1:n.312C>A
(DGUOK-AS1)
|
|
|
XM_005264173.2:c.472G>T
(DGUOK)
|
XP_005264230.1:p.Asp158Tyr
|
|
XM_005264174.1:c.472G>T
(DGUOK)
|
XP_005264231.1:p.Asp158Tyr
|
|
XM_011532647.1:c.745G>T
(DGUOK)
|
XP_011530949.1:p.Asp249Tyr
|
|
XM_011532648.1:c.454G>T
(DGUOK)
|
XP_011530950.1:p.Asp152Tyr
|
|
XR_244926.2:n.728G>T
(DGUOK)
|
|
|
NM_001318859.1:c.481G>T
(DGUOK)
|
NP_001305788.1:p.Asp161Tyr
|
|
NM_001318860.1:c.472G>T
(DGUOK)
|
NP_001305789.1:p.Asp158Tyr
|
|
NM_001318861.1:c.472G>T
(DGUOK)
|
NP_001305790.1:p.Asp158Tyr
|
|
NM_001318862.1:c.454G>T
(DGUOK)
|
NP_001305791.1:p.Asp152Tyr
|
|
NM_001318863.1:c.454G>T
(DGUOK)
|
NP_001305792.1:p.Asp152Tyr
|
|
NR_134893.1:n.471G>T
(DGUOK)
|
|
|
NR_134894.1:n.619G>T
(DGUOK)
|
|
|
NR_134895.1:n.283G>T
(DGUOK)
|
|
|
NR_134896.1:n.453G>T
(DGUOK)
|
|
|
NR_134897.1:n.663G>T
(DGUOK)
|
|
|
NR_134898.1:n.587G>T
(DGUOK)
|
|
|
XM_011532647.2:c.745G>T
(DGUOK)
|
XP_011530949.1:p.Asp249Tyr
|
|
XM_024452739.1:c.472G>T
(DGUOK)
|
XP_024308507.1:p.Asp158Tyr
|
|
XR_001738656.1:n.699G>T
(DGUOK)
|
|
|
XR_244926.3:n.730G>T
(DGUOK)
|
|
|
NM_080916.3:c.763G>T
(DGUOK)
MANE Select
|
NP_550438.1:p.Asp255Tyr
|
|
NM_001318859.2:c.481G>T
(DGUOK)
|
NP_001305788.1:p.Asp161Tyr
|
|
NM_001318860.2:c.472G>T
(DGUOK)
|
NP_001305789.1:p.Asp158Tyr
|
|
NM_001318861.2:c.472G>T
(DGUOK)
|
NP_001305790.1:p.Asp158Tyr
|
|
NM_001318862.2:c.454G>T
(DGUOK)
|
NP_001305791.1:p.Asp152Tyr
|
|
NM_001318863.2:c.454G>T
(DGUOK)
|
NP_001305792.1:p.Asp152Tyr
|
|
NM_080918.3:c.499G>T
(DGUOK)
|
NP_550440.1:p.Asp167Tyr
|
|
NR_134893.2:n.417G>T
(DGUOK)
|
|
|
NR_134894.2:n.565G>T
(DGUOK)
|
|
|
NR_134895.2:n.229G>T
(DGUOK)
|
|
|
NR_134896.2:n.399G>T
(DGUOK)
|
|
|
NR_134897.2:n.609G>T
(DGUOK)
|
|
|
NR_134898.2:n.533G>T
(DGUOK)
|
|
|