|
NM_001363.5:c.1350G>T
MANE Select
|
NP_001354.1:p.Glu450Asp
|
|
ENST00000369550.10:c.1350G>T
MANE Select
|
ENSP00000358563.5:p.Glu450Asp
|
|
NM_001142463.2:c.1335G>T
|
NP_001135935.1:p.Glu445Asp
|
|
NM_001142463.3:c.1335G>T
|
NP_001135935.1:p.Glu445Asp
|
|
NM_001288747.1:c.*576G>T
|
NP_001275676.1:n.*576G>T
|
|
NM_001288747.2:c.*576G>T
|
NP_001275676.1:n.*576G>T
|
|
NM_001363.4:c.1350G>T
|
NP_001354.1:p.Glu450Asp
|
|
NR_110021.1:n.2051G>T
|
|
|
NR_110021.2:n.1929G>T
|
|
|
NR_110022.1:n.2170G>T
|
|
|
NR_110022.2:n.2048G>T
|
|
|
NR_110023.1:n.1944G>T
|
|
|
NR_110023.2:n.1822G>T
|
|
|
ENST00000369550.9:c.1350G>T
|
ENSP00000358563.5:p.Glu450Asp
|
|
ENST00000412124.5:c.608G>T
|
|
|
ENST00000413910.6:c.*146G>T
|
ENSP00000400542.2:n.*146G>T
|
|
ENST00000426673.5:c.769G>T
|
|
|
ENST00000426673.6:c.*792G>T
|
ENSP00000407253.3:n.*792G>T
|
|
ENST00000475966.1:n.839G>T
|
|
|
ENST00000484317.6:n.1624G>T
|
|
|
ENST00000492372.1:n.167G>T
|
|
|
ENST00000492372.2:n.288G>T
|
|
|
ENST00000620277.4:c.*576G>T
|
ENSP00000478387.1:n.*576G>T
|
|
ENST00000696575.1:c.1335G>T
|
ENSP00000512730.1:p.Glu445Asp
|
|
ENST00000696577.1:c.1350G>T
|
ENSP00000512731.1:p.Glu450Asp
|
|
ENST00000696578.1:c.*302G>T
|
ENSP00000512732.1:n.*302G>T
|
|
ENST00000696579.1:n.2365G>T
|
|
|
ENST00000696580.1:c.1263G>T
|
ENSP00000512733.1:p.Glu421Asp
|
|
ENST00000696581.1:c.*1324G>T
|
ENSP00000512734.1:n.*1324G>T
|
|
ENST00000696582.1:c.*556G>T
|
ENSP00000512735.1:n.*556G>T
|
|
ENST00000696583.1:c.1311G>T
|
ENSP00000512736.1:p.Glu437Asp
|
|
ENST00000696584.1:n.1874G>T
|
|
|
ENST00000696585.1:n.1993G>T
|
|
|
ENST00000696586.1:n.1767G>T
|
|
|
ENST00000696587.1:c.1230G>T
|
ENSP00000512737.1:p.Glu410Asp
|
|
ENST00000696588.1:c.741G>T
|
ENSP00000513251.1:p.Glu247Asp
|
|
ENST00000696589.1:n.1125G>T
|
|
|
ENST00000696590.1:n.2376G>T
|
|
|
ENST00000696591.1:n.699G>T
|
|
|
ENST00000696592.1:n.3631G>T
|
|
|
ENST00000696627.1:c.*176G>T
|
ENSP00000512764.1:n.*176G>T
|
|
ENST00000696628.1:c.1350G>T
|
ENSP00000512765.1:p.Glu450Asp
|
