|
ENST00000176643.11:c.1345G>C
MANE Select
|
ENSP00000176643.6:p.Asp449His
|
|
|
ENST00000395575.7:c.1018G>C
|
ENSP00000378942.3:p.Asp340His
|
|
|
ENST00000472059.6:c.*903G>C
|
ENSP00000458397.1:n.*903G>C
|
|
|
ENST00000571163.2:c.227-3638G>C
|
ENSP00000459977.2:n.227-3638G>C
|
|
|
ENST00000573947.2:c.145G>C
|
ENSP00000462933.2:p.Asp49His
|
|
|
ENST00000574078.3:n.674G>C
|
|
|
|
ENST00000581518.6:c.1345G>C
|
ENSP00000461916.2:p.Asp449His
|
|
|
ENST00000582991.6:c.*63G>C
|
ENSP00000464153.1:n.*63G>C
|
|
|
ENST00000671878.1:c.1345G>C
|
ENSP00000500516.1:p.Asp449His
|
|
|
ENST00000672059.1:n.1696G>C
|
|
|
|
ENST00000672357.1:c.1345G>C
|
ENSP00000500092.1:p.Asp449His
|
|
|
ENST00000672465.1:c.1345G>C
|
ENSP00000500517.1:p.Asp449His
|
|
|
ENST00000672487.1:c.*525G>C
|
ENSP00000500740.1:n.*525G>C
|
|
|
ENST00000672564.1:n.3014G>C
|
|
|
|
ENST00000672567.1:c.1098+6811G>C
|
|
|
|
ENST00000672591.1:c.405G>C
|
|
|
|
ENST00000672608.1:n.2334G>C
|
|
|
|
ENST00000672709.1:c.1199G>C
|
|
|
|
ENST00000673064.1:n.1845G>C
|
|
|
|
ENST00000673136.1:c.1208-3638G>C
|
ENSP00000500380.1:n.1208-3638G>C
|
|
|
ENST00000673472.1:n.1681G>C
|
|
|
|
ENST00000673516.1:n.1805G>C
|
|
|
|
ENST00000176643.10:c.1345G>C
|
ENSP00000176643.6:p.Asp449His
|
|
|
ENST00000339618.8:c.1345G>C
|
ENSP00000345774.4:p.Asp449His
|
|
|
ENST00000395575.6:c.1345G>C
|
ENSP00000378942.2:p.Asp449His
|
|
|
ENST00000472059.5:c.*903G>C
|
ENSP00000458397.1:n.*903G>C
|
|
|
ENST00000476965.5:n.1095G>C
|
|
|
|
ENST00000571163.1:c.227-3700G>C
|
ENSP00000459977.1:n.227-3700G>C
|
|
|
ENST00000573565.1:c.60G>C
|
|
|
|
ENST00000573947.1:c.252G>C
|
ENSP00000462933.1:n.252G>C
|
|
|
ENST00000575384.2:c.91G>C
|
ENSP00000461235.2:p.Asp31His
|
|
|
ENST00000579855.5:c.1345G>C
|
ENSP00000463637.1:p.Asp449His
|
|
|
ENST00000581518.5:c.1345G>C
|
ENSP00000461916.1:p.Asp449His
|
|
|
ENST00000582991.5:c.*63G>C
|
ENSP00000464153.1:n.*63G>C
|
|
|
ENST00000630662.2:c.227-3700G>C
|
ENSP00000487353.1:n.227-3700G>C
|
|
|
ENST00000631291.2:c.*63G>C
|
ENSP00000486085.1:n.*63G>C
|
|
|
NM_000382.2:c.1345G>C
|
NP_000373.1:p.Asp449His
|
|
|
NM_001031806.1:c.1345G>C
|
NP_001026976.1:p.Asp449His
|
|
|
XM_011523732.1:c.1345G>C
|
XP_011522034.1:p.Asp449His
|
|
|
XM_011523733.1:c.1345G>C
|
XP_011522035.1:p.Asp449His
|
|
|
XM_011523733.2:c.1345G>C
|
XP_011522035.1:p.Asp449His
|
|
|
XM_017024355.1:c.1208-3700G>C
|
XP_016879844.1:n.1208-3700G>C
|
|
|
XM_017024356.2:c.1345G>C
|
XP_016879845.1:p.Asp449His
|
|
|
XM_017024357.1:c.1345G>C
|
XP_016879846.1:p.Asp449His
|
|
|
XM_017024358.2:c.1208-3700G>C
|
XP_016879847.1:n.1208-3700G>C
|
|
|
XM_024450651.1:c.766G>C
|
XP_024306419.1:p.Asp256His
|
|
|
XM_024450652.1:c.766G>C
|
XP_024306420.1:p.Asp256His
|
|
|
NM_000382.3:c.1345G>C
MANE Select
|
NP_000373.1:p.Asp449His
|
|
|
NM_001031806.2:c.1345G>C
|
NP_001026976.1:p.Asp449His
|
|
|
NM_001369136.1:c.1345G>C
|
NP_001356065.1:p.Asp449His
|
|
|
NM_001369137.1:c.1345G>C
|
NP_001356066.1:p.Asp449His
|
|
|
NM_001369138.1:c.1345G>C
|
NP_001356067.1:p.Asp449His
|
|
|
NM_001369139.1:c.1345G>C
|
NP_001356068.1:p.Asp449His
|
|
|
NM_001369146.1:c.1208-3700G>C
|
NP_001356075.1:n.1208-3700G>C
|
|
|
NM_001369148.1:c.766G>C
|
NP_001356077.1:p.Asp256His
|
|
|
NM_001369137.2:c.1345G>C
|
NP_001356066.1:p.Asp449His
|
|
|
NM_001369138.2:c.1345G>C
|
NP_001356067.1:p.Asp449His
|
|
|
NM_001369146.2:c.1208-3700G>C
|
NP_001356075.1:n.1208-3700G>C
|
|
|
NM_001369148.2:c.766G>C
|
NP_001356077.1:p.Asp256His
|
|
