ENST00000509514.6:c.577G=
|
ENSP00000426272.2:p.Ala193=
|
|
ENST00000518349.6:c.113-17567G=
|
ENSP00000507185.1:n.113-17567G=
|
|
ENST00000682445.1:c.*458G=
|
ENSP00000508061.1:n.*458G=
|
|
ENST00000682531.1:n.678G=
|
|
|
ENST00000682626.1:c.*83G=
|
ENSP00000507857.1:n.*83G=
|
|
ENST00000682996.1:c.577G=
|
ENSP00000507792.1:p.Ala193=
|
|
ENST00000683265.1:n.670G=
|
|
|
ENST00000683371.1:c.*707G=
|
ENSP00000508376.1:n.*707G=
|
|
ENST00000683390.1:n.2267G=
|
|
|
ENST00000683549.1:n.498G=
|
|
|
ENST00000683936.1:c.*462G=
|
ENSP00000507721.1:n.*462G=
|
|
ENST00000683974.1:n.659G=
|
|
|
ENST00000683996.1:c.166G=
|
ENSP00000507060.1:p.Ala56=
|
|
ENST00000684131.1:n.416G=
|
|
|
ENST00000684160.1:c.*267G=
|
ENSP00000507821.1:n.*267G=
|
|
ENST00000684214.1:c.577G=
|
ENSP00000508071.1:p.Ala193=
|
|
ENST00000414835.7:c.652G=
|
ENSP00000411960.3:p.Ala218=
|
|
ENST00000510025.7:c.577G=
MANE Select
|
ENSP00000424940.3:p.Ala193=
|
|
ENST00000643250.1:c.*449G=
|
ENSP00000494737.1:n.*449G=
|
|
ENST00000644146.1:c.*155G=
|
ENSP00000494808.1:n.*155G=
|
|
ENST00000645099.1:c.136G=
|
ENSP00000496091.1:p.Ala46=
|
|
ENST00000645702.1:c.166G=
|
ENSP00000496432.1:p.Ala56=
|
|
ENST00000645832.1:c.*462G=
|
ENSP00000494316.1:n.*462G=
|
|
ENST00000646058.1:c.577G=
|
ENSP00000493579.1:p.Ala193=
|
|
ENST00000646355.1:c.*583G=
|
ENSP00000493801.1:n.*583G=
|
|
ENST00000646554.1:c.*555G=
|
ENSP00000494542.1:n.*555G=
|
|
ENST00000647335.1:c.*544G=
|
ENSP00000495180.1:n.*544G=
|
|
ENST00000647342.1:c.*508G=
|
ENSP00000494992.1:n.*508G=
|
|
ENST00000256216.10:c.577G=
|
ENSP00000256216.6:p.Ala193=
|
|
ENST00000414835.6:c.157G=
|
ENSP00000411960.2:p.Ala53=
|
|
ENST00000442060.7:c.577G=
|
ENSP00000390208.3:p.Ala193=
|
|
ENST00000503168.5:n.566G=
|
|
|
ENST00000504811.5:c.652G=
|
ENSP00000420914.1:p.Ala218=
|
|
ENST00000505181.5:n.280G=
|
|
|
ENST00000509514.5:c.-308G=
|
ENSP00000426272.1:n.-308G=
|
|
ENST00000510025.5:c.505G=
|
ENSP00000424940.1:p.Ala169=
|
|
ENST00000512644.1:n.145G=
|
|
|
ENST00000513628.5:c.166G=
|
ENSP00000425993.1:p.Ala56=
|
|
ENST00000515235.6:n.637G=
|
|
|
ENST00000515320.5:c.523G=
|
ENSP00000424613.1:p.Ala175=
|
|
NM_000414.3:c.577G=
|
NP_000405.1:p.Ala193=
|
|
NM_001199291.2:c.652G=
|
NP_001186220.1:p.Ala218=
|
|
NM_001199292.1:c.523G=
|
NP_001186221.1:p.Ala175=
|
|
NM_001292027.1:c.505G=
|
NP_001278956.1:p.Ala169=
|
|
NM_001292028.1:c.157G=
|
NP_001278957.1:p.Ala53=
|
|
NM_000414.4:c.577G=
MANE Select
|
NP_000405.1:p.Ala193=
|
|
NM_001199291.3:c.652G=
|
NP_001186220.1:p.Ala218=
|
|
NM_001199292.2:c.523G=
|
NP_001186221.1:p.Ala175=
|
|
NM_001292027.2:c.505G=
|
NP_001278956.1:p.Ala169=
|
|
NM_001292028.2:c.157G=
|
NP_001278957.1:p.Ala53=
|
|
NM_001374497.1:c.568G=
|
NP_001361426.1:p.Ala190=
|
|
NM_001374498.1:c.577G=
|
NP_001361427.1:p.Ala193=
|
|
NM_001374499.1:c.250G=
|
NP_001361428.1:p.Ala84=
|
|
NM_001374500.1:c.136G=
|
NP_001361429.1:p.Ala46=
|
|
NM_001374501.1:c.166G=
|
NP_001361430.1:p.Ala56=
|
|
NM_001374502.1:c.166G=
|
NP_001361431.1:p.Ala56=
|
|
NM_001374503.1:c.166G=
|
NP_001361432.1:p.Ala56=
|
|
NR_164653.1:n.656G=
|
|
|
NR_164654.1:n.844G=
|
|
|