|
ENST00000509514.6:c.1606A>G
|
ENSP00000426272.2:p.Ile536Val
|
|
|
ENST00000518349.6:c.919A>G
|
ENSP00000507185.1:p.Ile307Val
|
|
|
ENST00000520244.6:n.3413A>G
|
|
|
|
ENST00000682445.1:c.*1556A>G
|
ENSP00000508061.1:n.*1556A>G
|
|
|
ENST00000682531.1:n.3567A>G
|
|
|
|
ENST00000682626.1:c.*1181A>G
|
ENSP00000507857.1:n.*1181A>G
|
|
|
ENST00000682996.1:c.1603A>G
|
ENSP00000507792.1:p.Ile535Val
|
|
|
ENST00000683265.1:n.3461A>G
|
|
|
|
ENST00000683335.1:n.3077A>G
|
|
|
|
ENST00000683371.1:c.*1805A>G
|
ENSP00000508376.1:n.*1805A>G
|
|
|
ENST00000683372.1:n.3685A>G
|
|
|
|
ENST00000683390.1:n.3365A>G
|
|
|
|
ENST00000683476.1:n.517A>G
|
|
|
|
ENST00000683549.1:n.3289A>G
|
|
|
|
ENST00000683936.1:c.*3253A>G
|
ENSP00000507721.1:n.*3253A>G
|
|
|
ENST00000683974.1:n.3404A>G
|
|
|
|
ENST00000683996.1:c.*885A>G
|
ENSP00000507060.1:n.*885A>G
|
|
|
ENST00000684131.1:n.3207A>G
|
|
|
|
ENST00000684160.1:c.*1365A>G
|
ENSP00000507821.1:n.*1365A>G
|
|
|
ENST00000684214.1:c.1675A>G
|
ENSP00000508071.1:p.Ile559Val
|
|
|
ENST00000414835.7:c.1750A>G
|
ENSP00000411960.3:p.Ile584Val
|
|
|
ENST00000510025.7:c.1675A>G
MANE Select
|
ENSP00000424940.3:p.Ile559Val
|
|
|
ENST00000643250.1:c.*1547A>G
|
ENSP00000494737.1:n.*1547A>G
|
|
|
ENST00000644146.1:c.*2946A>G
|
ENSP00000494808.1:n.*2946A>G
|
|
|
ENST00000645099.1:c.1234A>G
|
ENSP00000496091.1:p.Ile412Val
|
|
|
ENST00000645702.1:c.*1078A>G
|
ENSP00000496432.1:n.*1078A>G
|
|
|
ENST00000645832.1:c.*1560A>G
|
ENSP00000494316.1:n.*1560A>G
|
|
|
ENST00000646058.1:c.1675A>G
|
ENSP00000493579.1:p.Ile559Val
|
|
|
ENST00000646355.1:c.*1681A>G
|
ENSP00000493801.1:n.*1681A>G
|
|
|
ENST00000646554.1:c.*1653A>G
|
ENSP00000494542.1:n.*1653A>G
|
|
|
ENST00000647335.1:c.*1642A>G
|
ENSP00000495180.1:n.*1642A>G
|
|
|
ENST00000647342.1:c.*1606A>G
|
ENSP00000494992.1:n.*1606A>G
|
|
|
ENST00000256216.10:c.1675A>G
|
ENSP00000256216.6:p.Ile559Val
|
|
|
ENST00000414835.6:c.1255A>G
|
ENSP00000411960.2:p.Ile419Val
|
|
|
ENST00000442060.7:c.*237A>G
|
ENSP00000390208.3:n.*237A>G
|
|
|
ENST00000504811.5:c.1750A>G
|
ENSP00000420914.1:p.Ile584Val
|
|
|
ENST00000507353.1:n.283A>G
|
|
|
|
ENST00000509514.5:c.889A>G
|
ENSP00000426272.1:p.Ile297Val
|
|
|
ENST00000509951.5:n.130A>G
|
|
|
|
ENST00000510025.5:c.1603A>G
|
ENSP00000424940.1:p.Ile535Val
|
|
|
ENST00000513628.5:c.1264A>G
|
ENSP00000425993.1:p.Ile422Val
|
|
|
ENST00000515235.6:n.3428A>G
|
|
|
|
ENST00000515320.5:c.1621A>G
|
ENSP00000424613.1:p.Ile541Val
|
|
|
ENST00000518349.5:n.809A>G
|
|
|
|
ENST00000522415.5:n.342A>G
|
|
|
|
NM_000414.3:c.1675A>G
|
NP_000405.1:p.Ile559Val
|
|
|
NM_001199291.2:c.1750A>G
|
NP_001186220.1:p.Ile584Val
|
|
|
NM_001199292.1:c.1621A>G
|
NP_001186221.1:p.Ile541Val
|
|
|
NM_001292027.1:c.1603A>G
|
NP_001278956.1:p.Ile535Val
|
|
|
NM_001292028.1:c.1255A>G
|
NP_001278957.1:p.Ile419Val
|
|
|
NM_000414.4:c.1675A>G
MANE Select
|
NP_000405.1:p.Ile559Val
|
|
|
NM_001199291.3:c.1750A>G
|
NP_001186220.1:p.Ile584Val
|
|
|
NM_001199292.2:c.1621A>G
|
NP_001186221.1:p.Ile541Val
|
|
|
NM_001292027.2:c.1603A>G
|
NP_001278956.1:p.Ile535Val
|
|
|
NM_001292028.2:c.1255A>G
|
NP_001278957.1:p.Ile419Val
|
|
|
NM_001374497.1:c.1666A>G
|
NP_001361426.1:p.Ile556Val
|
|
|
NM_001374498.1:c.1603A>G
|
NP_001361427.1:p.Ile535Val
|
|
|
NM_001374499.1:c.1348A>G
|
NP_001361428.1:p.Ile450Val
|
|
|
NM_001374500.1:c.1234A>G
|
NP_001361429.1:p.Ile412Val
|
|
|
NM_001374501.1:c.1264A>G
|
NP_001361430.1:p.Ile422Val
|
|
|
NM_001374502.1:c.1264A>G
|
NP_001361431.1:p.Ile422Val
|
|
|
NM_001374503.1:c.1264A>G
|
NP_001361432.1:p.Ile422Val
|
|
|
NR_164653.1:n.1772A>G
|
|
|
|
NR_164654.1:n.2040A>G
|
|
|
