ENST00000413910.6:c.748G>C
|
ENSP00000400542.2:p.Glu250Gln
|
|
ENST00000426673.6:c.*251G>C
|
ENSP00000407253.3:n.*251G>C
|
|
ENST00000484317.6:n.653G>C
|
|
|
ENST00000696575.1:c.868G>C
|
ENSP00000512730.1:p.Glu290Gln
|
|
ENST00000696576.1:n.970G>C
|
|
|
ENST00000696577.1:c.868G>C
|
ENSP00000512731.1:p.Glu290Gln
|
|
ENST00000696578.1:c.868G>C
|
ENSP00000512732.1:p.Glu290Gln
|
|
ENST00000696579.1:n.970G>C
|
|
|
ENST00000696580.1:c.781G>C
|
ENSP00000512733.1:p.Glu261Gln
|
|
ENST00000696581.1:c.*842G>C
|
ENSP00000512734.1:n.*842G>C
|
|
ENST00000696582.1:c.*74G>C
|
ENSP00000512735.1:n.*74G>C
|
|
ENST00000696583.1:c.829G>C
|
ENSP00000512736.1:p.Glu277Gln
|
|
ENST00000696584.1:n.1392G>C
|
|
|
ENST00000696585.1:n.1511G>C
|
|
|
ENST00000696586.1:n.1285G>C
|
|
|
ENST00000696587.1:c.748G>C
|
ENSP00000512737.1:p.Glu250Gln
|
|
ENST00000696588.1:c.259G>C
|
ENSP00000513251.1:p.Glu87Gln
|
|
ENST00000696589.1:n.643G>C
|
|
|
ENST00000696590.1:n.492G>C
|
|
|
ENST00000696591.1:n.217G>C
|
|
|
ENST00000696627.1:c.868G>C
|
ENSP00000512764.1:p.Glu290Gln
|
|
ENST00000696628.1:c.868G>C
|
ENSP00000512765.1:p.Glu290Gln
|
|
ENST00000369550.10:c.868G>C
MANE Select
|
ENSP00000358563.5:p.Glu290Gln
|
|
ENST00000369550.9:c.868G>C
|
ENSP00000358563.5:p.Glu290Gln
|
|
ENST00000412124.5:c.174-1496G>C
|
|
|
ENST00000413910.5:c.748G>C
|
ENSP00000400542.1:p.Glu250Gln
|
|
ENST00000426673.5:c.228G>C
|
|
|
ENST00000475966.1:n.357G>C
|
|
|
ENST00000484317.5:n.506G>C
|
|
|
ENST00000620277.4:c.868G>C
|
ENSP00000478387.1:p.Glu290Gln
|
|
NM_001142463.2:c.868G>C
|
NP_001135935.1:p.Glu290Gln
|
|
NM_001288747.1:c.868G>C
|
NP_001275676.1:p.Glu290Gln
|
|
NM_001363.4:c.868G>C
|
NP_001354.1:p.Glu290Gln
|
|
NR_110021.1:n.1569G>C
|
|
|
NR_110022.1:n.1688G>C
|
|
|
NR_110023.1:n.1462G>C
|
|
|
NM_001363.5:c.868G>C
MANE Select
|
NP_001354.1:p.Glu290Gln
|
|
NM_001142463.3:c.868G>C
|
NP_001135935.1:p.Glu290Gln
|
|
NR_110021.2:n.1447G>C
|
|
|
NR_110022.2:n.1566G>C
|
|
|
NR_110023.2:n.1340G>C
|
|
|
NM_001288747.2:c.868G>C
|
NP_001275676.1:p.Glu290Gln
|
|