|
NM_021155.4:c.642G>T
MANE Select
|
NP_066978.1:p.Glu214Asp
|
|
ENST00000315599.12:c.642G>T
MANE Select
|
ENSP00000315477.6:p.Glu214Asp
|
|
NM_001144893.1:c.340+170G>T
|
NP_001138365.1:n.340+170G>T
|
|
NM_001144893.2:c.340+170G>T
|
NP_001138365.1:n.340+170G>T
|
|
NM_001144894.1:c.510G>T
|
NP_001138366.1:p.Glu170Asp
|
|
NM_001144894.2:c.510G>T
|
NP_001138366.1:p.Glu170Asp
|
|
NM_001144895.1:c.472+170G>T
|
NP_001138367.1:n.472+170G>T
|
|
NM_001144895.2:c.472+170G>T
|
NP_001138367.1:n.472+170G>T
|
|
NM_001144896.1:c.570G>T
|
NP_001138368.1:p.Glu190Asp
|
|
NM_001144896.2:c.570G>T
|
NP_001138368.1:p.Glu190Asp
|
|
NM_001144897.1:c.642G>T
|
NP_001138369.1:p.Glu214Asp
|
|
NM_001144897.2:c.642G>T
|
NP_001138369.1:p.Glu214Asp
|
|
NM_001144899.1:c.265+377G>T
|
NP_001138371.1:n.265+377G>T
|
|
NM_001144899.2:c.265+377G>T
|
NP_001138371.1:n.265+377G>T
|
|
NM_021155.3:c.642G>T
|
NP_066978.1:p.Glu214Asp
|
|
NR_026692.1:n.809G>T
|
|
|
NR_026692.2:n.765G>T
|
|
|
ENST00000204801.12:c.510G>T
|
ENSP00000204801.7:p.Glu170Asp
|
|
ENST00000315591.12:c.570G>T
|
ENSP00000315407.7:p.Glu190Asp
|
|
ENST00000315599.11:c.642G>T
|
ENSP00000315477.6:p.Glu214Asp
|
|
ENST00000354397.10:c.642G>T
|
ENSP00000346373.5:p.Glu214Asp
|
|
ENST00000394161.9:c.218+424G>T
|
ENSP00000377716.4:n.218+424G>T
|
|
ENST00000394173.8:c.265+377G>T
|
ENSP00000377728.4:n.265+377G>T
|
|
ENST00000593660.5:c.538+32G>T
|
ENSP00000470530.1:n.538+32G>T
|
|
ENST00000593821.5:c.340+170G>T
|
ENSP00000471348.1:n.340+170G>T
|
|
ENST00000601256.1:c.570G>T
|
ENSP00000470658.1:p.Glu190Asp
|
|
ENST00000601951.5:c.570G>T
|
ENSP00000468827.1:p.Glu190Asp
|
|
ENST00000602261.5:c.472+170G>T
|
ENSP00000471137.1:n.472+170G>T
|
|
ENST00000678003.1:c.39G>T
|
ENSP00000504497.1:p.Glu13Asp
|
|
XM_005272472.3:c.334+308G>T
|
XP_005272529.1:n.334+308G>T
|
|
XM_005272472.4:c.334+308G>T
|
XP_005272529.1:n.334+308G>T
|
