ENST00000264093.9:c.760G>T
(DGUOK)
MANE Select
|
ENSP00000264093.4:p.Asp254Tyr
|
|
ENST00000264093.8:c.760G>T
(DGUOK)
|
ENSP00000264093.4:p.Asp254Tyr
|
|
ENST00000348222.3:c.496G>T
(DGUOK)
|
ENSP00000306964.3:p.Asp166Tyr
|
|
ENST00000418996.5:c.*113G>T
(DGUOK)
|
ENSP00000408209.1:n.*113G>T
|
|
ENST00000462685.1:n.589G>T
(DGUOK)
|
|
|
ENST00000489796.5:n.645G>T
(DGUOK)
|
|
|
ENST00000629438.2:c.*377G>T
(DGUOK)
|
ENSP00000487122.1:n.*377G>T
|
|
NM_080916.2:c.760G>T
(DGUOK)
|
NP_550438.1:p.Asp254Tyr
|
|
NM_080918.2:c.496G>T
(DGUOK)
|
NP_550440.1:p.Asp166Tyr
|
|
NR_104029.1:n.341C>A
(DGUOK-AS1)
|
|
|
NR_104030.1:n.315C>A
(DGUOK-AS1)
|
|
|
XM_005264173.2:c.469G>T
(DGUOK)
|
XP_005264230.1:p.Asp157Tyr
|
|
XM_005264174.1:c.469G>T
(DGUOK)
|
XP_005264231.1:p.Asp157Tyr
|
|
XM_011532647.1:c.742G>T
(DGUOK)
|
XP_011530949.1:p.Asp248Tyr
|
|
XM_011532648.1:c.451G>T
(DGUOK)
|
XP_011530950.1:p.Asp151Tyr
|
|
XR_244926.2:n.725G>T
(DGUOK)
|
|
|
NM_001318859.1:c.478G>T
(DGUOK)
|
NP_001305788.1:p.Asp160Tyr
|
|
NM_001318860.1:c.469G>T
(DGUOK)
|
NP_001305789.1:p.Asp157Tyr
|
|
NM_001318861.1:c.469G>T
(DGUOK)
|
NP_001305790.1:p.Asp157Tyr
|
|
NM_001318862.1:c.451G>T
(DGUOK)
|
NP_001305791.1:p.Asp151Tyr
|
|
NM_001318863.1:c.451G>T
(DGUOK)
|
NP_001305792.1:p.Asp151Tyr
|
|
NR_134893.1:n.468G>T
(DGUOK)
|
|
|
NR_134894.1:n.616G>T
(DGUOK)
|
|
|
NR_134895.1:n.280G>T
(DGUOK)
|
|
|
NR_134896.1:n.450G>T
(DGUOK)
|
|
|
NR_134897.1:n.660G>T
(DGUOK)
|
|
|
NR_134898.1:n.584G>T
(DGUOK)
|
|
|
XM_011532647.2:c.742G>T
(DGUOK)
|
XP_011530949.1:p.Asp248Tyr
|
|
XM_024452739.1:c.469G>T
(DGUOK)
|
XP_024308507.1:p.Asp157Tyr
|
|
XR_001738656.1:n.696G>T
(DGUOK)
|
|
|
XR_244926.3:n.727G>T
(DGUOK)
|
|
|
NM_080916.3:c.760G>T
(DGUOK)
MANE Select
|
NP_550438.1:p.Asp254Tyr
|
|
NM_001318859.2:c.478G>T
(DGUOK)
|
NP_001305788.1:p.Asp160Tyr
|
|
NM_001318860.2:c.469G>T
(DGUOK)
|
NP_001305789.1:p.Asp157Tyr
|
|
NM_001318861.2:c.469G>T
(DGUOK)
|
NP_001305790.1:p.Asp157Tyr
|
|
NM_001318862.2:c.451G>T
(DGUOK)
|
NP_001305791.1:p.Asp151Tyr
|
|
NM_001318863.2:c.451G>T
(DGUOK)
|
NP_001305792.1:p.Asp151Tyr
|
|
NM_080918.3:c.496G>T
(DGUOK)
|
NP_550440.1:p.Asp166Tyr
|
|
NR_134893.2:n.414G>T
(DGUOK)
|
|
|
NR_134894.2:n.562G>T
(DGUOK)
|
|
|
NR_134895.2:n.226G>T
(DGUOK)
|
|
|
NR_134896.2:n.396G>T
(DGUOK)
|
|
|
NR_134897.2:n.606G>T
(DGUOK)
|
|
|
NR_134898.2:n.530G>T
(DGUOK)
|
|
|