|
ENST00000509514.6:c.470G>T
|
ENSP00000426272.2:p.Gly157Val
|
|
|
ENST00000518349.6:c.113-17674G>T
|
ENSP00000507185.1:n.113-17674G>T
|
|
|
ENST00000682445.1:c.*351G>T
|
ENSP00000508061.1:n.*351G>T
|
|
|
ENST00000682531.1:n.571G>T
|
|
|
|
ENST00000682626.1:c.498G>T
|
ENSP00000507857.1:p.Trp166Cys
|
|
|
ENST00000682996.1:c.470G>T
|
ENSP00000507792.1:p.Gly157Val
|
|
|
ENST00000683265.1:n.563G>T
|
|
|
|
ENST00000683371.1:c.*600G>T
|
ENSP00000508376.1:n.*600G>T
|
|
|
ENST00000683390.1:n.2160G>T
|
|
|
|
ENST00000683549.1:n.391G>T
|
|
|
|
ENST00000683936.1:c.*355G>T
|
ENSP00000507721.1:n.*355G>T
|
|
|
ENST00000683974.1:n.552G>T
|
|
|
|
ENST00000683996.1:c.59G>T
|
ENSP00000507060.1:p.Gly20Val
|
|
|
ENST00000684131.1:n.309G>T
|
|
|
|
ENST00000684160.1:c.*160G>T
|
ENSP00000507821.1:n.*160G>T
|
|
|
ENST00000684214.1:c.470G>T
|
ENSP00000508071.1:p.Gly157Val
|
|
|
ENST00000414835.7:c.545G>T
|
ENSP00000411960.3:p.Gly182Val
|
|
|
ENST00000510025.7:c.470G>T
MANE Select
|
ENSP00000424940.3:p.Gly157Val
|
|
|
ENST00000643250.1:c.*342G>T
|
ENSP00000494737.1:n.*342G>T
|
|
|
ENST00000644146.1:c.*48G>T
|
ENSP00000494808.1:n.*48G>T
|
|
|
ENST00000645099.1:c.29G>T
|
ENSP00000496091.1:p.Gly10Val
|
|
|
ENST00000645702.1:c.59G>T
|
ENSP00000496432.1:p.Gly20Val
|
|
|
ENST00000645832.1:c.*355G>T
|
ENSP00000494316.1:n.*355G>T
|
|
|
ENST00000646058.1:c.470G>T
|
ENSP00000493579.1:p.Gly157Val
|
|
|
ENST00000646355.1:c.*476G>T
|
ENSP00000493801.1:n.*476G>T
|
|
|
ENST00000646554.1:c.*448G>T
|
ENSP00000494542.1:n.*448G>T
|
|
|
ENST00000646590.1:c.461G>T
|
ENSP00000494892.1:p.Gly154Val
|
|
|
ENST00000647335.1:c.*437G>T
|
ENSP00000495180.1:n.*437G>T
|
|
|
ENST00000647342.1:c.*401G>T
|
ENSP00000494992.1:n.*401G>T
|
|
|
ENST00000256216.10:c.470G>T
|
ENSP00000256216.6:p.Gly157Val
|
|
|
ENST00000414835.6:c.50G>T
|
ENSP00000411960.2:p.Gly17Val
|
|
|
ENST00000442060.7:c.470G>T
|
ENSP00000390208.3:p.Gly157Val
|
|
|
ENST00000503168.5:n.459G>T
|
|
|
|
ENST00000504811.5:c.545G>T
|
ENSP00000420914.1:p.Gly182Val
|
|
|
ENST00000505181.5:n.173G>T
|
|
|
|
ENST00000508788.5:n.372G>T
|
|
|
|
ENST00000509514.5:c.-415G>T
|
ENSP00000426272.1:n.-415G>T
|
|
|
ENST00000510025.5:c.398G>T
|
ENSP00000424940.1:p.Gly133Val
|
|
|
ENST00000512644.1:n.38G>T
|
|
|
|
ENST00000512841.5:n.518G>T
|
|
|
|
ENST00000513628.5:c.59G>T
|
ENSP00000425993.1:p.Gly20Val
|
|
|
ENST00000515235.6:n.530G>T
|
|
|
|
ENST00000515320.5:c.416G>T
|
ENSP00000424613.1:p.Gly139Val
|
|
|
NM_000414.3:c.470G>T
|
NP_000405.1:p.Gly157Val
|
|
|
NM_001199291.2:c.545G>T
|
NP_001186220.1:p.Gly182Val
|
|
|
NM_001199292.1:c.416G>T
|
NP_001186221.1:p.Gly139Val
|
|
|
NM_001292027.1:c.398G>T
|
NP_001278956.1:p.Gly133Val
|
|
|
NM_001292028.1:c.50G>T
|
NP_001278957.1:p.Gly17Val
|
|
|
NM_000414.4:c.470G>T
MANE Select
|
NP_000405.1:p.Gly157Val
|
|
|
NM_001199291.3:c.545G>T
|
NP_001186220.1:p.Gly182Val
|
|
|
NM_001199292.2:c.416G>T
|
NP_001186221.1:p.Gly139Val
|
|
|
NM_001292027.2:c.398G>T
|
NP_001278956.1:p.Gly133Val
|
|
|
NM_001292028.2:c.50G>T
|
NP_001278957.1:p.Gly17Val
|
|
|
NM_001374497.1:c.461G>T
|
NP_001361426.1:p.Gly154Val
|
|
|
NM_001374498.1:c.470G>T
|
NP_001361427.1:p.Gly157Val
|
|
|
NM_001374499.1:c.143G>T
|
NP_001361428.1:p.Gly48Val
|
|
|
NM_001374500.1:c.29G>T
|
NP_001361429.1:p.Gly10Val
|
|
|
NM_001374501.1:c.59G>T
|
NP_001361430.1:p.Gly20Val
|
|
|
NM_001374502.1:c.59G>T
|
NP_001361431.1:p.Gly20Val
|
|
|
NM_001374503.1:c.59G>T
|
NP_001361432.1:p.Gly20Val
|
|
|
NR_164653.1:n.549G>T
|
|
|
|
NR_164654.1:n.737G>T
|
|
|
