|
ENST00000509514.6:c.1905A>T
|
ENSP00000426272.2:p.Gly635=
|
|
|
ENST00000518349.6:c.1218A>T
|
ENSP00000507185.1:p.Gly406=
|
|
|
ENST00000682445.1:c.*1855A>T
|
ENSP00000508061.1:n.*1855A>T
|
|
|
ENST00000682531.1:n.3866A>T
|
|
|
|
ENST00000682626.1:c.*1480A>T
|
ENSP00000507857.1:n.*1480A>T
|
|
|
ENST00000682996.1:c.1902A>T
|
ENSP00000507792.1:p.Gly634=
|
|
|
ENST00000683265.1:n.3760A>T
|
|
|
|
ENST00000683335.1:n.3376A>T
|
|
|
|
ENST00000683371.1:c.*2104A>T
|
ENSP00000508376.1:n.*2104A>T
|
|
|
ENST00000683372.1:n.3984A>T
|
|
|
|
ENST00000683390.1:n.3664A>T
|
|
|
|
ENST00000683476.1:n.816A>T
|
|
|
|
ENST00000683549.1:n.3588A>T
|
|
|
|
ENST00000683936.1:c.*3552A>T
|
ENSP00000507721.1:n.*3552A>T
|
|
|
ENST00000683974.1:n.3703A>T
|
|
|
|
ENST00000683996.1:c.*1184A>T
|
ENSP00000507060.1:n.*1184A>T
|
|
|
ENST00000684131.1:n.3506A>T
|
|
|
|
ENST00000684160.1:c.*1664A>T
|
ENSP00000507821.1:n.*1664A>T
|
|
|
ENST00000684214.1:c.1854+1405A>T
|
ENSP00000508071.1:n.1854+1405A>T
|
|
|
ENST00000414835.7:c.2049A>T
|
ENSP00000411960.3:p.Gly683=
|
|
|
ENST00000510025.7:c.1974A>T
MANE Select
|
ENSP00000424940.3:p.Gly658=
|
|
|
ENST00000643250.1:c.*1846A>T
|
ENSP00000494737.1:n.*1846A>T
|
|
|
ENST00000644146.1:c.*3245A>T
|
ENSP00000494808.1:n.*3245A>T
|
|
|
ENST00000645099.1:c.1533A>T
|
ENSP00000496091.1:p.Gly511=
|
|
|
ENST00000645702.1:c.*1377A>T
|
ENSP00000496432.1:n.*1377A>T
|
|
|
ENST00000645832.1:c.*1859A>T
|
ENSP00000494316.1:n.*1859A>T
|
|
|
ENST00000646058.1:c.1974A>T
|
ENSP00000493579.1:p.Gly658=
|
|
|
ENST00000646355.1:c.*1980A>T
|
ENSP00000493801.1:n.*1980A>T
|
|
|
ENST00000646554.1:c.*1952A>T
|
ENSP00000494542.1:n.*1952A>T
|
|
|
ENST00000647335.1:c.*1941A>T
|
ENSP00000495180.1:n.*1941A>T
|
|
|
ENST00000647342.1:c.*1905A>T
|
ENSP00000494992.1:n.*1905A>T
|
|
|
ENST00000256216.10:c.1974A>T
|
ENSP00000256216.6:p.Gly658=
|
|
|
ENST00000414835.6:c.1554A>T
|
ENSP00000411960.2:p.Gly518=
|
|
|
ENST00000442060.7:c.*529A>T
|
ENSP00000390208.3:n.*529A>T
|
|
|
ENST00000504811.5:c.2049A>T
|
ENSP00000420914.1:p.Gly683=
|
|
|
ENST00000509514.5:c.1188A>T
|
ENSP00000426272.1:p.Gly396=
|
|
|
ENST00000509606.1:n.269A>T
|
|
|
|
ENST00000509951.5:n.309+1405A>T
|
|
|
|
ENST00000510025.5:c.1902A>T
|
ENSP00000424940.1:p.Gly634=
|
|
|
ENST00000513628.5:c.1563A>T
|
ENSP00000425993.1:p.Gly521=
|
|
|
ENST00000515235.6:n.3727A>T
|
|
|
|
ENST00000515320.5:c.1920A>T
|
ENSP00000424613.1:p.Gly640=
|
|
|
ENST00000522415.5:n.641A>T
|
|
|
|
NM_000414.3:c.1974A>T
|
NP_000405.1:p.Gly658=
|
|
|
NM_001199291.2:c.2049A>T
|
NP_001186220.1:p.Gly683=
|
|
|
NM_001199292.1:c.1920A>T
|
NP_001186221.1:p.Gly640=
|
|
|
NM_001292027.1:c.1902A>T
|
NP_001278956.1:p.Gly634=
|
|
|
NM_001292028.1:c.1554A>T
|
NP_001278957.1:p.Gly518=
|
|
|
NM_000414.4:c.1974A>T
MANE Select
|
NP_000405.1:p.Gly658=
|
|
|
NM_001199291.3:c.2049A>T
|
NP_001186220.1:p.Gly683=
|
|
|
NM_001199292.2:c.1920A>T
|
NP_001186221.1:p.Gly640=
|
|
|
NM_001292027.2:c.1902A>T
|
NP_001278956.1:p.Gly634=
|
|
|
NM_001292028.2:c.1554A>T
|
NP_001278957.1:p.Gly518=
|
|
|
NM_001374497.1:c.1965A>T
|
NP_001361426.1:p.Gly655=
|
|
|
NM_001374498.1:c.1902A>T
|
NP_001361427.1:p.Gly634=
|
|
|
NM_001374499.1:c.1647A>T
|
NP_001361428.1:p.Gly549=
|
|
|
NM_001374500.1:c.1533A>T
|
NP_001361429.1:p.Gly511=
|
|
|
NM_001374501.1:c.1563A>T
|
NP_001361430.1:p.Gly521=
|
|
|
NM_001374502.1:c.1563A>T
|
NP_001361431.1:p.Gly521=
|
|
|
NM_001374503.1:c.1563A>T
|
NP_001361432.1:p.Gly521=
|
|
|
NR_164653.1:n.2071A>T
|
|
|
|
NR_164654.1:n.2339A>T
|
|
|
