|
ENST00000176643.11:c.1444-1G>T
MANE Select
|
ENSP00000176643.6:n.1444-1G>T
|
|
|
ENST00000395575.7:c.1117-1G>T
|
ENSP00000378942.3:n.1117-1G>T
|
|
|
ENST00000472059.6:c.*1006-5G>T
|
ENSP00000458397.1:n.*1006-5G>T
|
|
|
ENST00000571163.2:c.231-5G>T
|
ENSP00000459977.2:n.231-5G>T
|
|
|
ENST00000573947.2:c.248-5G>T
|
ENSP00000462933.2:n.248-5G>T
|
|
|
ENST00000574078.3:n.898-1G>T
|
|
|
|
ENST00000581518.6:c.1444-1G>T
|
ENSP00000461916.2:n.1444-1G>T
|
|
|
ENST00000582991.6:c.*162-1G>T
|
ENSP00000464153.1:n.*162-1G>T
|
|
|
ENST00000671878.1:c.1443+3601G>T
|
ENSP00000500516.1:n.1443+3601G>T
|
|
|
ENST00000672059.1:n.1795-1G>T
|
|
|
|
ENST00000672357.1:c.1444-1G>T
|
ENSP00000500092.1:n.1444-1G>T
|
|
|
ENST00000672465.1:c.1443+3601G>T
|
ENSP00000500517.1:n.1443+3601G>T
|
|
|
ENST00000672487.1:c.*628-5G>T
|
ENSP00000500740.1:n.*628-5G>T
|
|
|
ENST00000672564.1:n.3117-5G>T
|
|
|
|
ENST00000672567.1:c.1099-9718G>T
|
|
|
|
ENST00000672591.1:c.633-5G>T
|
|
|
|
ENST00000672608.1:n.2433-1G>T
|
|
|
|
ENST00000673136.1:c.1212-5G>T
|
ENSP00000500380.1:n.1212-5G>T
|
|
|
ENST00000673472.1:n.1784-5G>T
|
|
|
|
ENST00000673516.1:n.1904-1G>T
|
|
|
|
ENST00000176643.10:c.1444-1G>T
|
ENSP00000176643.6:n.1444-1G>T
|
|
|
ENST00000339618.8:c.*42-1G>T
|
ENSP00000345774.4:n.*42-1G>T
|
|
|
ENST00000395575.6:c.1444-1G>T
|
ENSP00000378942.2:n.1444-1G>T
|
|
|
ENST00000472059.5:c.*1002-1G>T
|
ENSP00000458397.1:n.*1002-1G>T
|
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|
ENST00000476965.5:n.1194-1G>T
|
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|
|
ENST00000571163.1:c.227-1G>T
|
ENSP00000459977.1:n.227-1G>T
|
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|
ENST00000573505.1:n.1474G>T
|
|
|
|
ENST00000573565.1:c.228-1G>T
|
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|
ENST00000573947.1:c.351-1G>T
|
ENSP00000462933.1:n.351-1G>T
|
|
|
ENST00000574597.1:n.206-1G>T
|
|
|
|
ENST00000575384.2:c.270-5G>T
|
ENSP00000461235.2:n.270-5G>T
|
|
|
ENST00000579855.5:c.1444-1G>T
|
ENSP00000463637.1:n.1444-1G>T
|
|
|
ENST00000581518.5:c.*46-5G>T
|
ENSP00000461916.1:n.*46-5G>T
|
|
|
ENST00000582991.5:c.*166-5G>T
|
ENSP00000464153.1:n.*166-5G>T
|
|
|
ENST00000630662.2:c.227-1G>T
|
ENSP00000487353.1:n.227-1G>T
|
|
|
ENST00000631291.2:c.*162-1G>T
|
ENSP00000486085.1:n.*162-1G>T
|
|
|
NM_000382.2:c.1444-1G>T
|
NP_000373.1:n.1444-1G>T
|
|
|
NM_001031806.1:c.*42-1G>T
|
NP_001026976.1:n.*42-1G>T
|
|
|
XM_011523732.1:c.*42-1G>T
|
XP_011522034.1:n.*42-1G>T
|
|
|
XM_011523733.1:c.*42-1G>T
|
XP_011522035.1:n.*42-1G>T
|
|
|
XM_011523733.2:c.*42-1G>T
|
XP_011522035.1:n.*42-1G>T
|
|
|
XM_017024355.1:c.1208-1G>T
|
XP_016879844.1:n.1208-1G>T
|
|
|
XM_017024356.2:c.1444-1G>T
|
XP_016879845.1:n.1444-1G>T
|
|
|
XM_017024357.1:c.1444-1G>T
|
XP_016879846.1:n.1444-1G>T
|
|
|
XM_017024358.2:c.1208-1G>T
|
XP_016879847.1:n.1208-1G>T
|
|
|
XM_024450651.1:c.*42-1G>T
|
XP_024306419.1:n.*42-1G>T
|
|
|
XM_024450652.1:c.865-1G>T
|
XP_024306420.1:n.865-1G>T
|
|
|
NM_000382.3:c.1444-1G>T
MANE Select
|
NP_000373.1:n.1444-1G>T
|
|
|
NM_001031806.2:c.*42-1G>T
|
NP_001026976.1:n.*42-1G>T
|
|
|
NM_001369136.1:c.*42-1G>T
|
NP_001356065.1:n.*42-1G>T
|
|
|
NM_001369137.1:c.*42-1G>T
|
NP_001356066.1:n.*42-1G>T
|
|
|
NM_001369138.1:c.1444-1G>T
|
NP_001356067.1:n.1444-1G>T
|
|
|
NM_001369139.1:c.1444-1G>T
|
NP_001356068.1:n.1444-1G>T
|
|
|
NM_001369146.1:c.1208-1G>T
|
NP_001356075.1:n.1208-1G>T
|
|
|
NM_001369148.1:c.865-1G>T
|
NP_001356077.1:n.865-1G>T
|
|
|
NM_001369137.2:c.*42-1G>T
|
NP_001356066.1:n.*42-1G>T
|
|
|
NM_001369138.2:c.1444-1G>T
|
NP_001356067.1:n.1444-1G>T
|
|
|
NM_001369146.2:c.1208-1G>T
|
NP_001356075.1:n.1208-1G>T
|
|
|
NM_001369148.2:c.865-1G>T
|
NP_001356077.1:n.865-1G>T
|
|
