ENST00000176643.11:c.1443+209G>T
MANE Select
|
ENSP00000176643.6:n.1443+209G>T
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ENST00000395575.7:c.1116+209G>T
|
ENSP00000378942.3:n.1116+209G>T
|
|
ENST00000472059.6:c.*1001+209G>T
|
ENSP00000458397.1:n.*1001+209G>T
|
|
ENST00000571163.2:c.227-3331G>T
|
ENSP00000459977.2:n.227-3331G>T
|
|
ENST00000573947.2:c.243+209G>T
|
ENSP00000462933.2:n.243+209G>T
|
|
ENST00000574078.3:n.772+209G>T
|
|
|
ENST00000581518.6:c.1443+209G>T
|
ENSP00000461916.2:n.1443+209G>T
|
|
ENST00000582991.6:c.*161+209G>T
|
ENSP00000464153.1:n.*161+209G>T
|
|
ENST00000671878.1:c.1443+209G>T
|
ENSP00000500516.1:n.1443+209G>T
|
|
ENST00000672059.1:n.1794+209G>T
|
|
|
ENST00000672357.1:c.1443+209G>T
|
ENSP00000500092.1:n.1443+209G>T
|
|
ENST00000672465.1:c.1443+209G>T
|
ENSP00000500517.1:n.1443+209G>T
|
|
ENST00000672487.1:c.*623+209G>T
|
ENSP00000500740.1:n.*623+209G>T
|
|
ENST00000672564.1:n.3112+209G>T
|
|
|
ENST00000672567.1:c.1098+7118G>T
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|
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ENST00000672591.1:c.503+209G>T
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ENST00000672608.1:n.2432+209G>T
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ENST00000672709.1:c.1297+209G>T
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|
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ENST00000673064.1:n.2152G>T
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|
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ENST00000673136.1:c.1208-3331G>T
|
ENSP00000500380.1:n.1208-3331G>T
|
|
ENST00000673472.1:n.1779+209G>T
|
|
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ENST00000673516.1:n.1903+209G>T
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|
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ENST00000176643.10:c.1443+209G>T
|
ENSP00000176643.6:n.1443+209G>T
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|
ENST00000339618.8:c.1443+209G>T
|
ENSP00000345774.4:n.1443+209G>T
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|
ENST00000395575.6:c.1443+209G>T
|
ENSP00000378942.2:n.1443+209G>T
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ENST00000472059.5:c.*1001+209G>T
|
ENSP00000458397.1:n.*1001+209G>T
|
|
ENST00000476965.5:n.1193+209G>T
|
|
|
ENST00000571163.1:c.227-3393G>T
|
ENSP00000459977.1:n.227-3393G>T
|
|
ENST00000573565.1:c.158+209G>T
|
|
|
ENST00000573947.1:c.350+209G>T
|
ENSP00000462933.1:n.350+209G>T
|
|
ENST00000575384.2:c.189+209G>T
|
ENSP00000461235.2:n.189+209G>T
|
|
ENST00000579855.5:c.1443+209G>T
|
ENSP00000463637.1:n.1443+209G>T
|
|
ENST00000581518.5:c.1443+209G>T
|
ENSP00000461916.1:n.1443+209G>T
|
|
ENST00000582991.5:c.*161+209G>T
|
ENSP00000464153.1:n.*161+209G>T
|
|
ENST00000630662.2:c.227-3393G>T
|
ENSP00000487353.1:n.227-3393G>T
|
|
ENST00000631291.2:c.*161+209G>T
|
ENSP00000486085.1:n.*161+209G>T
|
|
NM_000382.2:c.1443+209G>T
|
NP_000373.1:n.1443+209G>T
|
|
NM_001031806.1:c.1443+209G>T
|
NP_001026976.1:n.1443+209G>T
|
|
XM_011523732.1:c.1443+209G>T
|
XP_011522034.1:n.1443+209G>T
|
|
XM_011523733.1:c.1443+209G>T
|
XP_011522035.1:n.1443+209G>T
|
|
XM_011523733.2:c.1443+209G>T
|
XP_011522035.1:n.1443+209G>T
|
|
XM_017024355.1:c.1208-3393G>T
|
XP_016879844.1:n.1208-3393G>T
|
|
XM_017024356.2:c.1443+209G>T
|
XP_016879845.1:n.1443+209G>T
|
|
XM_017024357.1:c.1443+209G>T
|
XP_016879846.1:n.1443+209G>T
|
|
XM_017024358.2:c.1208-3393G>T
|
XP_016879847.1:n.1208-3393G>T
|
|
XM_024450651.1:c.864+209G>T
|
XP_024306419.1:n.864+209G>T
|
|
XM_024450652.1:c.864+209G>T
|
XP_024306420.1:n.864+209G>T
|
|
NM_000382.3:c.1443+209G>T
MANE Select
|
NP_000373.1:n.1443+209G>T
|
|
NM_001031806.2:c.1443+209G>T
|
NP_001026976.1:n.1443+209G>T
|
|
NM_001369136.1:c.1443+209G>T
|
NP_001356065.1:n.1443+209G>T
|
|
NM_001369137.1:c.1443+209G>T
|
NP_001356066.1:n.1443+209G>T
|
|
NM_001369138.1:c.1443+209G>T
|
NP_001356067.1:n.1443+209G>T
|
|
NM_001369139.1:c.1443+209G>T
|
NP_001356068.1:n.1443+209G>T
|
|
NM_001369146.1:c.1208-3393G>T
|
NP_001356075.1:n.1208-3393G>T
|
|
NM_001369148.1:c.864+209G>T
|
NP_001356077.1:n.864+209G>T
|
|
NM_001369137.2:c.1443+209G>T
|
NP_001356066.1:n.1443+209G>T
|
|
NM_001369138.2:c.1443+209G>T
|
NP_001356067.1:n.1443+209G>T
|
|
NM_001369146.2:c.1208-3393G>T
|
NP_001356075.1:n.1208-3393G>T
|
|
NM_001369148.2:c.864+209G>T
|
NP_001356077.1:n.864+209G>T
|
|