|
NM_002447.4:c.1477G>T
MANE Select
|
NP_002438.2:p.Asp493Tyr
|
|
ENST00000296474.8:c.1477G>T
MANE Select
|
ENSP00000296474.3:p.Asp493Tyr
|
|
NM_001244937.1:c.1477G>T
|
NP_001231866.1:p.Asp493Tyr
|
|
NM_001244937.2:c.1477G>T
|
NP_001231866.1:p.Asp493Tyr
|
|
NM_001244937.3:c.1477G>T
|
NP_001231866.1:p.Asp493Tyr
|
|
NM_001318913.1:c.1231-250G>T
|
NP_001305842.1:n.1231-250G>T
|
|
NM_001318913.2:c.1231-250G>T
|
NP_001305842.1:n.1231-250G>T
|
|
NM_002447.2:c.1477G>T
|
NP_002438.2:p.Asp493Tyr
|
|
NM_002447.3:c.1477G>T
|
NP_002438.2:p.Asp493Tyr
|
|
NR_134919.1:n.1505G>T
|
|
|
NR_134919.2:n.1741G>T
|
|
|
ENST00000296474.7:c.1477G>T
|
ENSP00000296474.3:p.Asp493Tyr
|
|
ENST00000344206.8:c.1477G>T
|
ENSP00000341325.4:p.Asp493Tyr
|
|
ENST00000411578.6:c.1477G>T
|
ENSP00000407926.2:p.Asp493Tyr
|
|
ENST00000468525.5:n.1477G>T
|
|
|
ENST00000485044.5:n.1477G>T
|
|
|
ENST00000493535.5:n.1231-250G>T
|
|
|
ENST00000612032.4:c.45+4627G>T
|
ENSP00000481084.1:n.45+4627G>T
|
|
ENST00000613534.4:c.712-3148G>T
|
ENSP00000482827.1:n.712-3148G>T
|
|
ENST00000621387.4:c.1231-250G>T
|
ENSP00000482642.1:n.1231-250G>T
|
|
XM_005265170.3:c.1477G>T
|
XP_005265227.2:p.Asp493Tyr
|
|
XM_005265170.4:c.1477G>T
|
XP_005265227.2:p.Asp493Tyr
|
|
XM_011533739.1:c.1477G>T
|
XP_011532041.1:p.Asp493Tyr
|
|
XM_011533739.2:c.1477G>T
|
XP_011532041.1:p.Asp493Tyr
|
|
XM_011533740.1:c.1477G>T
|
XP_011532042.1:p.Asp493Tyr
|
|
XM_011533740.2:c.1477G>T
|
XP_011532042.1:p.Asp493Tyr
|
|
XM_011533741.1:c.1477G>T
|
XP_011532043.1:p.Asp493Tyr
|
|
XM_011533741.2:c.1477G>T
|
XP_011532043.1:p.Asp493Tyr
|
|
XM_011533742.1:c.1477G>T
|
XP_011532044.1:p.Asp493Tyr
|
|
XM_011533742.2:c.1477G>T
|
XP_011532044.1:p.Asp493Tyr
|
|
XM_011533743.1:c.1477G>T
|
XP_011532045.1:p.Asp493Tyr
|
|
XM_011533743.2:c.1477G>T
|
XP_011532045.1:p.Asp493Tyr
|
|
XM_011533744.1:c.1231-250G>T
|
XP_011532046.1:n.1231-250G>T
|
|
XM_011533744.2:c.1231-250G>T
|
XP_011532046.1:n.1231-250G>T
|
|
XM_011533745.1:c.1231-250G>T
|
XP_011532047.1:n.1231-250G>T
|
|
XR_001740155.1:n.1500G>T
|
|
|
XR_245136.3:n.1503G>T
|
|
|
XR_940428.1:n.1503G>T
|
|
|
XR_940428.2:n.1500G>T
|
|
