|
ENST00000509514.6:c.1882G=
|
ENSP00000426272.2:p.Glu628=
|
|
|
ENST00000518349.6:c.1195G=
|
ENSP00000507185.1:p.Glu399=
|
|
|
ENST00000682445.1:c.*1832G=
|
ENSP00000508061.1:n.*1832G=
|
|
|
ENST00000682531.1:n.3843G=
|
|
|
|
ENST00000682626.1:c.*1457G=
|
ENSP00000507857.1:n.*1457G=
|
|
|
ENST00000682996.1:c.1879G=
|
ENSP00000507792.1:p.Glu627=
|
|
|
ENST00000683265.1:n.3737G=
|
|
|
|
ENST00000683335.1:n.3353G=
|
|
|
|
ENST00000683371.1:c.*2081G=
|
ENSP00000508376.1:n.*2081G=
|
|
|
ENST00000683372.1:n.3961G=
|
|
|
|
ENST00000683390.1:n.3641G=
|
|
|
|
ENST00000683476.1:n.793G=
|
|
|
|
ENST00000683549.1:n.3565G=
|
|
|
|
ENST00000683936.1:c.*3529G=
|
ENSP00000507721.1:n.*3529G=
|
|
|
ENST00000683974.1:n.3680G=
|
|
|
|
ENST00000683996.1:c.*1161G=
|
ENSP00000507060.1:n.*1161G=
|
|
|
ENST00000684131.1:n.3483G=
|
|
|
|
ENST00000684160.1:c.*1641G=
|
ENSP00000507821.1:n.*1641G=
|
|
|
ENST00000684214.1:c.1854+1382G=
|
ENSP00000508071.1:n.1854+1382G=
|
|
|
ENST00000414835.7:c.2026G=
|
ENSP00000411960.3:p.Glu676=
|
|
|
ENST00000510025.7:c.1951G=
MANE Select
|
ENSP00000424940.3:p.Glu651=
|
|
|
ENST00000643250.1:c.*1823G=
|
ENSP00000494737.1:n.*1823G=
|
|
|
ENST00000644146.1:c.*3222G=
|
ENSP00000494808.1:n.*3222G=
|
|
|
ENST00000645099.1:c.1510G=
|
ENSP00000496091.1:p.Glu504=
|
|
|
ENST00000645702.1:c.*1354G=
|
ENSP00000496432.1:n.*1354G=
|
|
|
ENST00000645832.1:c.*1836G=
|
ENSP00000494316.1:n.*1836G=
|
|
|
ENST00000646058.1:c.1951G=
|
ENSP00000493579.1:p.Glu651=
|
|
|
ENST00000646355.1:c.*1957G=
|
ENSP00000493801.1:n.*1957G=
|
|
|
ENST00000646554.1:c.*1929G=
|
ENSP00000494542.1:n.*1929G=
|
|
|
ENST00000647335.1:c.*1918G=
|
ENSP00000495180.1:n.*1918G=
|
|
|
ENST00000647342.1:c.*1882G=
|
ENSP00000494992.1:n.*1882G=
|
|
|
ENST00000256216.10:c.1951G=
|
ENSP00000256216.6:p.Glu651=
|
|
|
ENST00000414835.6:c.1531G=
|
ENSP00000411960.2:p.Glu511=
|
|
|
ENST00000442060.7:c.*506G=
|
ENSP00000390208.3:n.*506G=
|
|
|
ENST00000504811.5:c.2026G=
|
ENSP00000420914.1:p.Glu676=
|
|
|
ENST00000509514.5:c.1165G=
|
ENSP00000426272.1:p.Glu389=
|
|
|
ENST00000509606.1:n.246G=
|
|
|
|
ENST00000509951.5:n.309+1382G=
|
|
|
|
ENST00000510025.5:c.1879G=
|
ENSP00000424940.1:p.Glu627=
|
|
|
ENST00000513628.5:c.1540G=
|
ENSP00000425993.1:p.Glu514=
|
|
|
ENST00000515235.6:n.3704G=
|
|
|
|
ENST00000515320.5:c.1897G=
|
ENSP00000424613.1:p.Glu633=
|
|
|
ENST00000522415.5:n.618G=
|
|
|
|
NM_000414.3:c.1951G=
|
NP_000405.1:p.Glu651=
|
|
|
NM_001199291.2:c.2026G=
|
NP_001186220.1:p.Glu676=
|
|
|
NM_001199292.1:c.1897G=
|
NP_001186221.1:p.Glu633=
|
|
|
NM_001292027.1:c.1879G=
|
NP_001278956.1:p.Glu627=
|
|
|
NM_001292028.1:c.1531G=
|
NP_001278957.1:p.Glu511=
|
|
|
NM_000414.4:c.1951G=
MANE Select
|
NP_000405.1:p.Glu651=
|
|
|
NM_001199291.3:c.2026G=
|
NP_001186220.1:p.Glu676=
|
|
|
NM_001199292.2:c.1897G=
|
NP_001186221.1:p.Glu633=
|
|
|
NM_001292027.2:c.1879G=
|
NP_001278956.1:p.Glu627=
|
|
|
NM_001292028.2:c.1531G=
|
NP_001278957.1:p.Glu511=
|
|
|
NM_001374497.1:c.1942G=
|
NP_001361426.1:p.Glu648=
|
|
|
NM_001374498.1:c.1879G=
|
NP_001361427.1:p.Glu627=
|
|
|
NM_001374499.1:c.1624G=
|
NP_001361428.1:p.Glu542=
|
|
|
NM_001374500.1:c.1510G=
|
NP_001361429.1:p.Glu504=
|
|
|
NM_001374501.1:c.1540G=
|
NP_001361430.1:p.Glu514=
|
|
|
NM_001374502.1:c.1540G=
|
NP_001361431.1:p.Glu514=
|
|
|
NM_001374503.1:c.1540G=
|
NP_001361432.1:p.Glu514=
|
|
|
NR_164653.1:n.2048G=
|
|
|
|
NR_164654.1:n.2316G=
|
|
|
