|
ENST00000509514.6:c.462A>G
|
ENSP00000426272.2:p.Gly154=
|
|
|
ENST00000518349.6:c.113-17682A>G
|
ENSP00000507185.1:n.113-17682A>G
|
|
|
ENST00000682445.1:c.*343A>G
|
ENSP00000508061.1:n.*343A>G
|
|
|
ENST00000682531.1:n.563A>G
|
|
|
|
ENST00000682626.1:c.490A>G
|
ENSP00000507857.1:p.Asn164Asp
|
|
|
ENST00000682996.1:c.462A>G
|
ENSP00000507792.1:p.Gly154=
|
|
|
ENST00000683265.1:n.555A>G
|
|
|
|
ENST00000683371.1:c.*592A>G
|
ENSP00000508376.1:n.*592A>G
|
|
|
ENST00000683390.1:n.2152A>G
|
|
|
|
ENST00000683549.1:n.383A>G
|
|
|
|
ENST00000683936.1:c.*347A>G
|
ENSP00000507721.1:n.*347A>G
|
|
|
ENST00000683974.1:n.544A>G
|
|
|
|
ENST00000683996.1:c.51A>G
|
ENSP00000507060.1:p.Gly17=
|
|
|
ENST00000684131.1:n.301A>G
|
|
|
|
ENST00000684160.1:c.*152A>G
|
ENSP00000507821.1:n.*152A>G
|
|
|
ENST00000684214.1:c.462A>G
|
ENSP00000508071.1:p.Gly154=
|
|
|
ENST00000414835.7:c.537A>G
|
ENSP00000411960.3:p.Gly179=
|
|
|
ENST00000510025.7:c.462A>G
MANE Select
|
ENSP00000424940.3:p.Gly154=
|
|
|
ENST00000643250.1:c.*334A>G
|
ENSP00000494737.1:n.*334A>G
|
|
|
ENST00000644146.1:c.*40A>G
|
ENSP00000494808.1:n.*40A>G
|
|
|
ENST00000645099.1:c.21A>G
|
ENSP00000496091.1:p.Gly7=
|
|
|
ENST00000645702.1:c.51A>G
|
ENSP00000496432.1:p.Gly17=
|
|
|
ENST00000645832.1:c.*347A>G
|
ENSP00000494316.1:n.*347A>G
|
|
|
ENST00000646058.1:c.462A>G
|
ENSP00000493579.1:p.Gly154=
|
|
|
ENST00000646355.1:c.*468A>G
|
ENSP00000493801.1:n.*468A>G
|
|
|
ENST00000646554.1:c.*440A>G
|
ENSP00000494542.1:n.*440A>G
|
|
|
ENST00000646590.1:c.453A>G
|
ENSP00000494892.1:p.Gly151=
|
|
|
ENST00000647335.1:c.*429A>G
|
ENSP00000495180.1:n.*429A>G
|
|
|
ENST00000647342.1:c.*393A>G
|
ENSP00000494992.1:n.*393A>G
|
|
|
ENST00000256216.10:c.462A>G
|
ENSP00000256216.6:p.Gly154=
|
|
|
ENST00000414835.6:c.42A>G
|
ENSP00000411960.2:p.Gly14=
|
|
|
ENST00000442060.7:c.462A>G
|
ENSP00000390208.3:p.Gly154=
|
|
|
ENST00000503168.5:n.451A>G
|
|
|
|
ENST00000504811.5:c.537A>G
|
ENSP00000420914.1:p.Gly179=
|
|
|
ENST00000505181.5:n.165A>G
|
|
|
|
ENST00000508788.5:n.364A>G
|
|
|
|
ENST00000509514.5:c.-423A>G
|
ENSP00000426272.1:n.-423A>G
|
|
|
ENST00000510025.5:c.390A>G
|
ENSP00000424940.1:p.Gly130=
|
|
|
ENST00000512644.1:n.30A>G
|
|
|
|
ENST00000512841.5:n.510A>G
|
|
|
|
ENST00000513628.5:c.51A>G
|
ENSP00000425993.1:p.Gly17=
|
|
|
ENST00000515235.6:n.522A>G
|
|
|
|
ENST00000515320.5:c.408A>G
|
ENSP00000424613.1:p.Gly136=
|
|
|
NM_000414.3:c.462A>G
|
NP_000405.1:p.Gly154=
|
|
|
NM_001199291.2:c.537A>G
|
NP_001186220.1:p.Gly179=
|
|
|
NM_001199292.1:c.408A>G
|
NP_001186221.1:p.Gly136=
|
|
|
NM_001292027.1:c.390A>G
|
NP_001278956.1:p.Gly130=
|
|
|
NM_001292028.1:c.42A>G
|
NP_001278957.1:p.Gly14=
|
|
|
NM_000414.4:c.462A>G
MANE Select
|
NP_000405.1:p.Gly154=
|
|
|
NM_001199291.3:c.537A>G
|
NP_001186220.1:p.Gly179=
|
|
|
NM_001199292.2:c.408A>G
|
NP_001186221.1:p.Gly136=
|
|
|
NM_001292027.2:c.390A>G
|
NP_001278956.1:p.Gly130=
|
|
|
NM_001292028.2:c.42A>G
|
NP_001278957.1:p.Gly14=
|
|
|
NM_001374497.1:c.453A>G
|
NP_001361426.1:p.Gly151=
|
|
|
NM_001374498.1:c.462A>G
|
NP_001361427.1:p.Gly154=
|
|
|
NM_001374499.1:c.135A>G
|
NP_001361428.1:p.Gly45=
|
|
|
NM_001374500.1:c.21A>G
|
NP_001361429.1:p.Gly7=
|
|
|
NM_001374501.1:c.51A>G
|
NP_001361430.1:p.Gly17=
|
|
|
NM_001374502.1:c.51A>G
|
NP_001361431.1:p.Gly17=
|
|
|
NM_001374503.1:c.51A>G
|
NP_001361432.1:p.Gly17=
|
|
|
NR_164653.1:n.541A>G
|
|
|
|
NR_164654.1:n.729A>G
|
|
|
