ENST00000413910.6:c.1028G>A
|
ENSP00000400542.2:p.Gly343Asp
|
|
ENST00000426673.6:c.*531G>A
|
ENSP00000407253.3:n.*531G>A
|
|
ENST00000484317.6:n.933G>A
|
|
|
ENST00000696575.1:c.1148G>A
|
ENSP00000512730.1:p.Gly383Asp
|
|
ENST00000696577.1:c.1148G>A
|
ENSP00000512731.1:p.Gly383Asp
|
|
ENST00000696578.1:c.*100G>A
|
ENSP00000512732.1:n.*100G>A
|
|
ENST00000696579.1:n.1250G>A
|
|
|
ENST00000696580.1:c.1061G>A
|
ENSP00000512733.1:p.Gly354Asp
|
|
ENST00000696581.1:c.*1122G>A
|
ENSP00000512734.1:n.*1122G>A
|
|
ENST00000696582.1:c.*354G>A
|
ENSP00000512735.1:n.*354G>A
|
|
ENST00000696583.1:c.1109G>A
|
ENSP00000512736.1:p.Gly370Asp
|
|
ENST00000696584.1:n.1672G>A
|
|
|
ENST00000696585.1:n.1791G>A
|
|
|
ENST00000696586.1:n.1565G>A
|
|
|
ENST00000696587.1:c.1028G>A
|
ENSP00000512737.1:p.Gly343Asp
|
|
ENST00000696588.1:c.539G>A
|
ENSP00000513251.1:p.Gly180Asp
|
|
ENST00000696589.1:n.923G>A
|
|
|
ENST00000696590.1:n.772G>A
|
|
|
ENST00000696591.1:n.497G>A
|
|
|
ENST00000696592.1:n.2027G>A
|
|
|
ENST00000696627.1:c.1148G>A
|
ENSP00000512764.1:p.Gly383Asp
|
|
ENST00000696628.1:c.1148G>A
|
ENSP00000512765.1:p.Gly383Asp
|
|
ENST00000369550.10:c.1148G>A
MANE Select
|
ENSP00000358563.5:p.Gly383Asp
|
|
ENST00000369550.9:c.1148G>A
|
ENSP00000358563.5:p.Gly383Asp
|
|
ENST00000412124.5:c.406G>A
|
|
|
ENST00000426673.5:c.508G>A
|
|
|
ENST00000475966.1:n.637G>A
|
|
|
ENST00000481062.1:n.99G>A
|
|
|
ENST00000620277.4:c.1148G>A
|
ENSP00000478387.1:p.Gly383Asp
|
|
NM_001142463.2:c.1148G>A
|
NP_001135935.1:p.Gly383Asp
|
|
NM_001288747.1:c.1148G>A
|
NP_001275676.1:p.Gly383Asp
|
|
NM_001363.4:c.1148G>A
|
NP_001354.1:p.Gly383Asp
|
|
NR_110021.1:n.1849G>A
|
|
|
NR_110022.1:n.1968G>A
|
|
|
NR_110023.1:n.1742G>A
|
|
|
NM_001363.5:c.1148G>A
MANE Select
|
NP_001354.1:p.Gly383Asp
|
|
NM_001142463.3:c.1148G>A
|
NP_001135935.1:p.Gly383Asp
|
|
NR_110021.2:n.1727G>A
|
|
|
NR_110022.2:n.1846G>A
|
|
|
NR_110023.2:n.1620G>A
|
|
|
NM_001288747.2:c.1148G>A
|
NP_001275676.1:p.Gly383Asp
|
|