|
ENST00000340726.8:c.1090G>T
MANE Select
|
ENSP00000342626.3:p.Glu364Ter
|
|
|
ENST00000388741.7:c.988G>T
|
ENSP00000373393.2:p.Glu330Ter
|
|
|
ENST00000419131.6:c.1035+25087G>T
|
ENSP00000410176.1:n.1035+25087G>T
|
|
|
ENST00000465115.6:c.*369G>T
|
ENSP00000428391.1:n.*369G>T
|
|
|
ENST00000493349.2:c.326G>T
|
|
|
|
ENST00000496494.6:n.1553G>T
|
|
|
|
ENST00000642391.1:c.*817+25087G>T
|
ENSP00000496700.1:n.*817+25087G>T
|
|
|
ENST00000643681.1:c.1177G>T
|
ENSP00000495390.1:p.Glu393Ter
|
|
|
ENST00000644229.1:c.1122+25087G>T
|
ENSP00000494568.1:n.1122+25087G>T
|
|
|
ENST00000644424.1:n.160G>T
|
|
|
|
ENST00000644712.1:c.1119+25087G>T
|
ENSP00000496188.1:n.1119+25087G>T
|
|
|
ENST00000645793.1:c.1090G>T
|
ENSP00000496255.1:p.Glu364Ter
|
|
|
ENST00000647540.1:c.1090G>T
|
ENSP00000494438.1:p.Glu364Ter
|
|
|
ENST00000303824.11:c.1072G>T
|
ENSP00000303221.7:p.Glu358Ter
|
|
|
ENST00000340726.7:c.1090G>T
|
ENSP00000342626.3:p.Glu364Ter
|
|
|
ENST00000388740.4:c.991G>T
|
ENSP00000373392.3:p.Glu331Ter
|
|
|
ENST00000388741.6:c.988G>T
|
ENSP00000373393.2:p.Glu330Ter
|
|
|
ENST00000388742.8:c.1090G>T
|
ENSP00000373394.4:p.Glu364Ter
|
|
|
ENST00000388743.6:c.1087G>T
|
ENSP00000373395.2:p.Glu363Ter
|
|
|
ENST00000419131.5:c.1035+25087G>T
|
ENSP00000410176.1:n.1035+25087G>T
|
|
|
ENST00000465115.5:c.*369G>T
|
ENSP00000428391.1:n.*369G>T
|
|
|
ENST00000493349.1:c.7G>T
|
ENSP00000428517.1:p.Glu3Ter
|
|
|
ENST00000496494.5:n.1585G>T
|
|
|
|
NM_000503.5:c.1090G>T
|
NP_000494.2:p.Glu364Ter
|
|
|
NM_001288574.1:c.1072G>T
|
NP_001275503.1:p.Glu358Ter
|
|
|
NM_001288575.1:c.724G>T
|
NP_001275504.1:p.Glu242Ter
|
|
|
NM_172058.3:c.1090G>T
|
NP_742055.1:p.Glu364Ter
|
|
|
NM_172059.3:c.1035+25087G>T
|
NP_742056.1:n.1035+25087G>T
|
|
|
NM_172060.3:c.991G>T
|
NP_742057.1:p.Glu331Ter
|
|
|
XM_011517481.1:c.1162G>T
|
XP_011515783.1:p.Glu388Ter
|
|
|
XM_011517482.1:c.1177G>T
|
XP_011515784.1:p.Glu393Ter
|
|
|
XM_011517483.1:c.1087G>T
|
XP_011515785.1:p.Glu363Ter
|
|
|
XM_011517484.1:c.1075G>T
|
XP_011515786.1:p.Glu359Ter
|
|
|
XM_011517485.1:c.1090G>T
|
XP_011515787.1:p.Glu364Ter
|
|
|
XM_011517486.1:c.1090G>T
|
XP_011515788.1:p.Glu364Ter
|
|
|
XM_011517487.1:c.1090G>T
|
XP_011515789.1:p.Glu364Ter
|
|
|
XM_011517488.1:c.1087G>T
|
XP_011515790.1:p.Glu363Ter
|
|
|
XM_011517489.1:c.1027G>T
|
XP_011515791.1:p.Glu343Ter
|
|
|
XM_011517490.1:c.991G>T
|
XP_011515792.1:p.Glu331Ter
|
|
|
XM_011517491.1:c.991G>T
|
XP_011515793.1:p.Glu331Ter
|
|
|
XM_011517492.1:c.739G>T
|
XP_011515794.1:p.Glu247Ter
|
|
|
NM_172059.4:c.1122+25087G>T
|
NP_742056.2:n.1122+25087G>T
|
|
|
XM_011517483.2:c.1087G>T
|
XP_011515785.1:p.Glu363Ter
|
|
|
XM_011517484.3:c.1162G>T
|
XP_011515786.2:p.Glu388Ter
|
|
|
XM_017013201.1:c.1177G>T
|
XP_016868690.1:p.Glu393Ter
|
|
|
XM_017013202.1:c.1177G>T
|
XP_016868691.1:p.Glu393Ter
|
|
|
XM_017013203.2:c.1174G>T
|
XP_016868692.1:p.Glu392Ter
|
|
|
XM_017013204.2:c.1159G>T
|
XP_016868693.1:p.Glu387Ter
|
|
|
XM_017013205.2:c.1177G>T
|
XP_016868694.1:p.Glu393Ter
|
|
|
XM_017013206.1:c.1090G>T
|
XP_016868695.1:p.Glu364Ter
|
|
|
XM_017013207.2:c.1137+25087G>T
|
XP_016868696.1:n.1137+25087G>T
|
|
|
XM_017013208.2:c.1087G>T
|
XP_016868697.1:p.Glu363Ter
|
|
|
XM_017013210.2:c.1119+25087G>T
|
XP_016868699.1:n.1119+25087G>T
|
|
|
XM_017013211.2:c.1027G>T
|
XP_016868700.1:p.Glu343Ter
|
|
|
XM_017013212.2:c.991G>T
|
XP_016868701.1:p.Glu331Ter
|
|
|
XM_017013213.1:c.739G>T
|
XP_016868702.1:p.Glu247Ter
|
|
|
NM_000503.6:c.1090G>T
MANE Select
|
NP_000494.2:p.Glu364Ter
|
|
|
NM_001288574.2:c.1072G>T
|
NP_001275503.1:p.Glu358Ter
|
|
|
NM_001288575.2:c.724G>T
|
NP_001275504.1:p.Glu242Ter
|
|
|
NM_001370333.1:c.1177G>T
|
NP_001357262.1:p.Glu393Ter
|
|
|
NM_001370334.1:c.1090G>T
|
NP_001357263.1:p.Glu364Ter
|
|
|
NM_001370335.1:c.1090G>T
|
NP_001357264.1:p.Glu364Ter
|
|
|
NM_001370336.1:c.1119+25087G>T
|
NP_001357265.1:n.1119+25087G>T
|
|
|
NM_172058.4:c.1090G>T
|
NP_742055.1:p.Glu364Ter
|
|
|
NM_172059.5:c.1122+25087G>T
|
NP_742056.2:n.1122+25087G>T
|
|
