|
ENST00000176643.11:c.1299A>C
MANE Select
|
ENSP00000176643.6:p.Glu433Asp
|
|
|
ENST00000395575.7:c.972A>C
|
ENSP00000378942.3:p.Glu324Asp
|
|
|
ENST00000472059.6:c.*857A>C
|
ENSP00000458397.1:n.*857A>C
|
|
|
ENST00000571163.2:c.227-3684A>C
|
ENSP00000459977.2:n.227-3684A>C
|
|
|
ENST00000573947.2:c.99A>C
|
ENSP00000462933.2:p.Glu33Asp
|
|
|
ENST00000574078.3:n.628A>C
|
|
|
|
ENST00000581518.6:c.1299A>C
|
ENSP00000461916.2:p.Glu433Asp
|
|
|
ENST00000582991.6:c.*17A>C
|
ENSP00000464153.1:n.*17A>C
|
|
|
ENST00000671878.1:c.1299A>C
|
ENSP00000500516.1:p.Glu433Asp
|
|
|
ENST00000672059.1:n.1650A>C
|
|
|
|
ENST00000672357.1:c.1299A>C
|
ENSP00000500092.1:p.Glu433Asp
|
|
|
ENST00000672465.1:c.1299A>C
|
ENSP00000500517.1:p.Glu433Asp
|
|
|
ENST00000672487.1:c.*479A>C
|
ENSP00000500740.1:n.*479A>C
|
|
|
ENST00000672564.1:n.2968A>C
|
|
|
|
ENST00000672567.1:c.1098+6765A>C
|
|
|
|
ENST00000672591.1:c.359A>C
|
|
|
|
ENST00000672608.1:n.2288A>C
|
|
|
|
ENST00000672709.1:c.1153A>C
|
|
|
|
ENST00000673064.1:n.1799A>C
|
|
|
|
ENST00000673136.1:c.1208-3684A>C
|
ENSP00000500380.1:n.1208-3684A>C
|
|
|
ENST00000673472.1:n.1635A>C
|
|
|
|
ENST00000673516.1:n.1759A>C
|
|
|
|
ENST00000176643.10:c.1299A>C
|
ENSP00000176643.6:p.Glu433Asp
|
|
|
ENST00000339618.8:c.1299A>C
|
ENSP00000345774.4:p.Glu433Asp
|
|
|
ENST00000395575.6:c.1299A>C
|
ENSP00000378942.2:p.Glu433Asp
|
|
|
ENST00000472059.5:c.*857A>C
|
ENSP00000458397.1:n.*857A>C
|
|
|
ENST00000476965.5:n.1049A>C
|
|
|
|
ENST00000571163.1:c.227-3746A>C
|
ENSP00000459977.1:n.227-3746A>C
|
|
|
ENST00000573565.1:c.14A>C
|
|
|
|
ENST00000573947.1:c.206A>C
|
ENSP00000462933.1:n.206A>C
|
|
|
ENST00000575384.2:c.45A>C
|
ENSP00000461235.2:p.Glu15Asp
|
|
|
ENST00000579855.5:c.1299A>C
|
ENSP00000463637.1:p.Glu433Asp
|
|
|
ENST00000581518.5:c.1299A>C
|
ENSP00000461916.1:p.Glu433Asp
|
|
|
ENST00000582991.5:c.*17A>C
|
ENSP00000464153.1:n.*17A>C
|
|
|
ENST00000630662.2:c.227-3746A>C
|
ENSP00000487353.1:n.227-3746A>C
|
|
|
ENST00000631291.2:c.*17A>C
|
ENSP00000486085.1:n.*17A>C
|
|
|
NM_000382.2:c.1299A>C
|
NP_000373.1:p.Glu433Asp
|
|
|
NM_001031806.1:c.1299A>C
|
NP_001026976.1:p.Glu433Asp
|
|
|
XM_011523732.1:c.1299A>C
|
XP_011522034.1:p.Glu433Asp
|
|
|
XM_011523733.1:c.1299A>C
|
XP_011522035.1:p.Glu433Asp
|
|
|
XM_011523733.2:c.1299A>C
|
XP_011522035.1:p.Glu433Asp
|
|
|
XM_017024355.1:c.1208-3746A>C
|
XP_016879844.1:n.1208-3746A>C
|
|
|
XM_017024356.2:c.1299A>C
|
XP_016879845.1:p.Glu433Asp
|
|
|
XM_017024357.1:c.1299A>C
|
XP_016879846.1:p.Glu433Asp
|
|
|
XM_017024358.2:c.1208-3746A>C
|
XP_016879847.1:n.1208-3746A>C
|
|
|
XM_024450651.1:c.720A>C
|
XP_024306419.1:p.Glu240Asp
|
|
|
XM_024450652.1:c.720A>C
|
XP_024306420.1:p.Glu240Asp
|
|
|
NM_000382.3:c.1299A>C
MANE Select
|
NP_000373.1:p.Glu433Asp
|
|
|
NM_001031806.2:c.1299A>C
|
NP_001026976.1:p.Glu433Asp
|
|
|
NM_001369136.1:c.1299A>C
|
NP_001356065.1:p.Glu433Asp
|
|
|
NM_001369137.1:c.1299A>C
|
NP_001356066.1:p.Glu433Asp
|
|
|
NM_001369138.1:c.1299A>C
|
NP_001356067.1:p.Glu433Asp
|
|
|
NM_001369139.1:c.1299A>C
|
NP_001356068.1:p.Glu433Asp
|
|
|
NM_001369146.1:c.1208-3746A>C
|
NP_001356075.1:n.1208-3746A>C
|
|
|
NM_001369148.1:c.720A>C
|
NP_001356077.1:p.Glu240Asp
|
|
|
NM_001369137.2:c.1299A>C
|
NP_001356066.1:p.Glu433Asp
|
|
|
NM_001369138.2:c.1299A>C
|
NP_001356067.1:p.Glu433Asp
|
|
|
NM_001369146.2:c.1208-3746A>C
|
NP_001356075.1:n.1208-3746A>C
|
|
|
NM_001369148.2:c.720A>C
|
NP_001356077.1:p.Glu240Asp
|
|
