|
ENST00000509514.6:c.455C>G
|
ENSP00000426272.2:p.Ala152Gly
|
|
|
ENST00000518349.6:c.113-17689C>G
|
ENSP00000507185.1:n.113-17689C>G
|
|
|
ENST00000682445.1:c.*336C>G
|
ENSP00000508061.1:n.*336C>G
|
|
|
ENST00000682531.1:n.556C>G
|
|
|
|
ENST00000682626.1:c.483C>G
|
ENSP00000507857.1:p.Ser161Arg
|
|
|
ENST00000682996.1:c.455C>G
|
ENSP00000507792.1:p.Ala152Gly
|
|
|
ENST00000683265.1:n.548C>G
|
|
|
|
ENST00000683371.1:c.*585C>G
|
ENSP00000508376.1:n.*585C>G
|
|
|
ENST00000683390.1:n.2145C>G
|
|
|
|
ENST00000683549.1:n.376C>G
|
|
|
|
ENST00000683936.1:c.*340C>G
|
ENSP00000507721.1:n.*340C>G
|
|
|
ENST00000683974.1:n.537C>G
|
|
|
|
ENST00000683996.1:c.44C>G
|
ENSP00000507060.1:p.Ala15Gly
|
|
|
ENST00000684131.1:n.294C>G
|
|
|
|
ENST00000684160.1:c.*145C>G
|
ENSP00000507821.1:n.*145C>G
|
|
|
ENST00000684214.1:c.455C>G
|
ENSP00000508071.1:p.Ala152Gly
|
|
|
ENST00000414835.7:c.530C>G
|
ENSP00000411960.3:p.Ala177Gly
|
|
|
ENST00000510025.7:c.455C>G
MANE Select
|
ENSP00000424940.3:p.Ala152Gly
|
|
|
ENST00000643250.1:c.*327C>G
|
ENSP00000494737.1:n.*327C>G
|
|
|
ENST00000644146.1:c.*33C>G
|
ENSP00000494808.1:n.*33C>G
|
|
|
ENST00000645099.1:c.14C>G
|
ENSP00000496091.1:p.Ala5Gly
|
|
|
ENST00000645702.1:c.44C>G
|
ENSP00000496432.1:p.Ala15Gly
|
|
|
ENST00000645832.1:c.*340C>G
|
ENSP00000494316.1:n.*340C>G
|
|
|
ENST00000646058.1:c.455C>G
|
ENSP00000493579.1:p.Ala152Gly
|
|
|
ENST00000646355.1:c.*461C>G
|
ENSP00000493801.1:n.*461C>G
|
|
|
ENST00000646554.1:c.*433C>G
|
ENSP00000494542.1:n.*433C>G
|
|
|
ENST00000646590.1:c.446C>G
|
ENSP00000494892.1:p.Ala149Gly
|
|
|
ENST00000647335.1:c.*422C>G
|
ENSP00000495180.1:n.*422C>G
|
|
|
ENST00000647342.1:c.*386C>G
|
ENSP00000494992.1:n.*386C>G
|
|
|
ENST00000256216.10:c.455C>G
|
ENSP00000256216.6:p.Ala152Gly
|
|
|
ENST00000414835.6:c.35C>G
|
ENSP00000411960.2:p.Ala12Gly
|
|
|
ENST00000442060.7:c.455C>G
|
ENSP00000390208.3:p.Ala152Gly
|
|
|
ENST00000503168.5:n.444C>G
|
|
|
|
ENST00000504811.5:c.530C>G
|
ENSP00000420914.1:p.Ala177Gly
|
|
|
ENST00000505181.5:n.158C>G
|
|
|
|
ENST00000508788.5:n.357C>G
|
|
|
|
ENST00000509514.5:c.-430C>G
|
ENSP00000426272.1:n.-430C>G
|
|
|
ENST00000510025.5:c.383C>G
|
ENSP00000424940.1:p.Ala128Gly
|
|
|
ENST00000512644.1:n.23C>G
|
|
|
|
ENST00000512841.5:n.503C>G
|
|
|
|
ENST00000513628.5:c.44C>G
|
ENSP00000425993.1:p.Ala15Gly
|
|
|
ENST00000515235.6:n.515C>G
|
|
|
|
ENST00000515320.5:c.401C>G
|
ENSP00000424613.1:p.Ala134Gly
|
|
|
NM_000414.3:c.455C>G
|
NP_000405.1:p.Ala152Gly
|
|
|
NM_001199291.2:c.530C>G
|
NP_001186220.1:p.Ala177Gly
|
|
|
NM_001199292.1:c.401C>G
|
NP_001186221.1:p.Ala134Gly
|
|
|
NM_001292027.1:c.383C>G
|
NP_001278956.1:p.Ala128Gly
|
|
|
NM_001292028.1:c.35C>G
|
NP_001278957.1:p.Ala12Gly
|
|
|
NM_000414.4:c.455C>G
MANE Select
|
NP_000405.1:p.Ala152Gly
|
|
|
NM_001199291.3:c.530C>G
|
NP_001186220.1:p.Ala177Gly
|
|
|
NM_001199292.2:c.401C>G
|
NP_001186221.1:p.Ala134Gly
|
|
|
NM_001292027.2:c.383C>G
|
NP_001278956.1:p.Ala128Gly
|
|
|
NM_001292028.2:c.35C>G
|
NP_001278957.1:p.Ala12Gly
|
|
|
NM_001374497.1:c.446C>G
|
NP_001361426.1:p.Ala149Gly
|
|
|
NM_001374498.1:c.455C>G
|
NP_001361427.1:p.Ala152Gly
|
|
|
NM_001374499.1:c.128C>G
|
NP_001361428.1:p.Ala43Gly
|
|
|
NM_001374500.1:c.14C>G
|
NP_001361429.1:p.Ala5Gly
|
|
|
NM_001374501.1:c.44C>G
|
NP_001361430.1:p.Ala15Gly
|
|
|
NM_001374502.1:c.44C>G
|
NP_001361431.1:p.Ala15Gly
|
|
|
NM_001374503.1:c.44C>G
|
NP_001361432.1:p.Ala15Gly
|
|
|
NR_164653.1:n.534C>G
|
|
|
|
NR_164654.1:n.722C>G
|
|
|
