|
ENST00000176643.11:c.1402T>G
MANE Select
|
ENSP00000176643.6:p.Leu468Val
|
|
|
ENST00000395575.7:c.1075T>G
|
ENSP00000378942.3:p.Leu359Val
|
|
|
ENST00000472059.6:c.*960T>G
|
ENSP00000458397.1:n.*960T>G
|
|
|
ENST00000571163.2:c.227-3581T>G
|
ENSP00000459977.2:n.227-3581T>G
|
|
|
ENST00000573947.2:c.202T>G
|
ENSP00000462933.2:p.Leu68Val
|
|
|
ENST00000574078.3:n.731T>G
|
|
|
|
ENST00000581518.6:c.1402T>G
|
ENSP00000461916.2:p.Leu468Val
|
|
|
ENST00000582991.6:c.*120T>G
|
ENSP00000464153.1:n.*120T>G
|
|
|
ENST00000671878.1:c.1402T>G
|
ENSP00000500516.1:p.Leu468Val
|
|
|
ENST00000672059.1:n.1753T>G
|
|
|
|
ENST00000672357.1:c.1402T>G
|
ENSP00000500092.1:p.Leu468Val
|
|
|
ENST00000672465.1:c.1402T>G
|
ENSP00000500517.1:p.Leu468Val
|
|
|
ENST00000672487.1:c.*582T>G
|
ENSP00000500740.1:n.*582T>G
|
|
|
ENST00000672564.1:n.3071T>G
|
|
|
|
ENST00000672567.1:c.1098+6868T>G
|
|
|
|
ENST00000672591.1:c.462T>G
|
|
|
|
ENST00000672608.1:n.2391T>G
|
|
|
|
ENST00000672709.1:c.1256T>G
|
|
|
|
ENST00000673064.1:n.1902T>G
|
|
|
|
ENST00000673136.1:c.1208-3581T>G
|
ENSP00000500380.1:n.1208-3581T>G
|
|
|
ENST00000673472.1:n.1738T>G
|
|
|
|
ENST00000673516.1:n.1862T>G
|
|
|
|
ENST00000176643.10:c.1402T>G
|
ENSP00000176643.6:p.Leu468Val
|
|
|
ENST00000339618.8:c.1402T>G
|
ENSP00000345774.4:p.Leu468Val
|
|
|
ENST00000395575.6:c.1402T>G
|
ENSP00000378942.2:p.Leu468Val
|
|
|
ENST00000472059.5:c.*960T>G
|
ENSP00000458397.1:n.*960T>G
|
|
|
ENST00000476965.5:n.1152T>G
|
|
|
|
ENST00000571163.1:c.227-3643T>G
|
ENSP00000459977.1:n.227-3643T>G
|
|
|
ENST00000573565.1:c.117T>G
|
|
|
|
ENST00000573947.1:c.309T>G
|
ENSP00000462933.1:n.309T>G
|
|
|
ENST00000575384.2:c.148T>G
|
ENSP00000461235.2:p.Leu50Val
|
|
|
ENST00000579855.5:c.1402T>G
|
ENSP00000463637.1:p.Leu468Val
|
|
|
ENST00000581518.5:c.1402T>G
|
ENSP00000461916.1:p.Leu468Val
|
|
|
ENST00000582991.5:c.*120T>G
|
ENSP00000464153.1:n.*120T>G
|
|
|
ENST00000630662.2:c.227-3643T>G
|
ENSP00000487353.1:n.227-3643T>G
|
|
|
ENST00000631291.2:c.*120T>G
|
ENSP00000486085.1:n.*120T>G
|
|
|
NM_000382.2:c.1402T>G
|
NP_000373.1:p.Leu468Val
|
|
|
NM_001031806.1:c.1402T>G
|
NP_001026976.1:p.Leu468Val
|
|
|
XM_011523732.1:c.1402T>G
|
XP_011522034.1:p.Leu468Val
|
|
|
XM_011523733.1:c.1402T>G
|
XP_011522035.1:p.Leu468Val
|
|
|
XM_011523733.2:c.1402T>G
|
XP_011522035.1:p.Leu468Val
|
|
|
XM_017024355.1:c.1208-3643T>G
|
XP_016879844.1:n.1208-3643T>G
|
|
|
XM_017024356.2:c.1402T>G
|
XP_016879845.1:p.Leu468Val
|
|
|
XM_017024357.1:c.1402T>G
|
XP_016879846.1:p.Leu468Val
|
|
|
XM_017024358.2:c.1208-3643T>G
|
XP_016879847.1:n.1208-3643T>G
|
|
|
XM_024450651.1:c.823T>G
|
XP_024306419.1:p.Leu275Val
|
|
|
XM_024450652.1:c.823T>G
|
XP_024306420.1:p.Leu275Val
|
|
|
NM_000382.3:c.1402T>G
MANE Select
|
NP_000373.1:p.Leu468Val
|
|
|
NM_001031806.2:c.1402T>G
|
NP_001026976.1:p.Leu468Val
|
|
|
NM_001369136.1:c.1402T>G
|
NP_001356065.1:p.Leu468Val
|
|
|
NM_001369137.1:c.1402T>G
|
NP_001356066.1:p.Leu468Val
|
|
|
NM_001369138.1:c.1402T>G
|
NP_001356067.1:p.Leu468Val
|
|
|
NM_001369139.1:c.1402T>G
|
NP_001356068.1:p.Leu468Val
|
|
|
NM_001369146.1:c.1208-3643T>G
|
NP_001356075.1:n.1208-3643T>G
|
|
|
NM_001369148.1:c.823T>G
|
NP_001356077.1:p.Leu275Val
|
|
|
NM_001369137.2:c.1402T>G
|
NP_001356066.1:p.Leu468Val
|
|
|
NM_001369138.2:c.1402T>G
|
NP_001356067.1:p.Leu468Val
|
|
|
NM_001369146.2:c.1208-3643T>G
|
NP_001356075.1:n.1208-3643T>G
|
|
|
NM_001369148.2:c.823T>G
|
NP_001356077.1:p.Leu275Val
|
|
