ENST00000461574.2:c.5447A>T
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ENSP00000417241.2:p.Glu1816Val
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ENST00000470026.6:c.5450A>T
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ENSP00000419274.2:p.Glu1817Val
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ENST00000473961.6:c.5324A>T
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ENSP00000420201.2:p.Glu1775Val
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ENST00000476777.6:c.5444A>T
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ENSP00000417554.2:p.Glu1815Val
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ENST00000477152.6:c.5372A>T
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ENSP00000419988.2:p.Glu1791Val
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ENST00000478531.6:c.2138A>T
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ENSP00000420412.2:p.Glu713Val
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ENST00000489037.2:c.5372A>T
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ENSP00000420781.2:p.Glu1791Val
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ENST00000493919.6:c.2000A>T
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ENSP00000418819.2:p.Glu667Val
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ENST00000494123.6:c.5450A>T
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ENSP00000419103.2:p.Glu1817Val
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ENST00000497488.2:c.4562A>T
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ENSP00000418986.2:p.Glu1521Val
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ENST00000618469.2:c.5450A>T
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ENSP00000478114.2:p.Glu1817Val
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ENST00000634433.2:c.5327A>T
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ENSP00000489431.2:p.Glu1776Val
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ENST00000644379.2:c.5516A>T
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ENSP00000496570.2:p.Glu1839Val
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ENST00000644555.2:c.2000A>T
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ENSP00000494614.2:p.Glu667Val
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ENST00000652672.2:c.5309A>T
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ENSP00000498906.2:p.Glu1770Val
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ENST00000484087.6:c.2012A>T
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ENSP00000419481.2:p.Glu671Val
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ENST00000700081.1:n.1333A>T
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ENST00000700082.1:n.814A>T
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ENST00000357654.9:c.5450A>T
MANE Select
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ENSP00000350283.3:p.Glu1817Val
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ENST00000471181.7:c.5513A>T
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ENSP00000418960.2:p.Glu1838Val
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ENST00000644379.1:c.1837A>T
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|
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ENST00000352993.7:c.2024A>T
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ENSP00000312236.5:p.Glu675Val
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ENST00000357654.7:c.5450A>T
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ENSP00000350283.3:p.Glu1817Val
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ENST00000461221.5:c.*5233A>T
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ENSP00000418548.1:n.*5233A>T
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ENST00000468300.5:c.2064A>T
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ENSP00000417148.1:p.Arg688Ser
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ENST00000471181.6:c.5513A>T
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ENSP00000418960.2:p.Glu1838Val
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ENST00000491747.6:c.2138A>T
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ENSP00000420705.2:p.Glu713Val
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ENST00000493795.5:c.5309A>T
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ENSP00000418775.1:p.Glu1770Val
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ENST00000586385.5:c.380A>T
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ENSP00000465818.1:p.Glu127Val
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ENST00000591534.5:c.923A>T
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ENSP00000467329.1:p.Glu308Val
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ENST00000591849.5:c.149A>T
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ENSP00000465347.1:p.Glu50Val
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NM_007294.3:c.5450A>T , LRG_292t1:c.5450A>T
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NP_009225.1:p.Glu1817Val
|
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NM_007297.3:c.5309A>T
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NP_009228.2:p.Glu1770Val
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|
NM_007298.3:c.2138A>T
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NP_009229.2:p.Glu713Val
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NM_007299.3:c.2064A>T
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NP_009230.2:p.Arg688Ser
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NM_007300.3:c.5513A>T
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NP_009231.2:p.Glu1838Val
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NR_027676.1:n.5586A>T
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|
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NM_007294.4:c.5450A>T
MANE Select
|
NP_009225.1:p.Glu1817Val
|
|
NM_007297.4:c.5309A>T
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NP_009228.2:p.Glu1770Val
|
|
NM_007299.4:c.2064A>T
|
NP_009230.2:p.Arg688Ser
|
|
NM_007300.4:c.5513A>T
|
NP_009231.2:p.Glu1838Val
|
|
NR_027676.2:n.5627A>T
|
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