ENST00000461574.2:c.5579G=
|
ENSP00000417241.2:p.Ser1860=
|
|
ENST00000470026.6:c.5582G=
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ENSP00000419274.2:p.Ser1861=
|
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ENST00000473961.6:c.5456G=
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ENSP00000420201.2:p.Ser1819=
|
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ENST00000476777.6:c.5576G=
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ENSP00000417554.2:p.Ser1859=
|
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ENST00000477152.6:c.5504G=
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ENSP00000419988.2:p.Ser1835=
|
|
ENST00000478531.6:c.2270G=
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ENSP00000420412.2:p.Ser757=
|
|
ENST00000489037.2:c.5504G=
|
ENSP00000420781.2:p.Ser1835=
|
|
ENST00000493919.6:c.2132G=
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ENSP00000418819.2:p.Ser711=
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ENST00000494123.6:c.5582G=
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ENSP00000419103.2:p.Ser1861=
|
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ENST00000497488.2:c.4694G=
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ENSP00000418986.2:p.Ser1565=
|
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ENST00000618469.2:c.5582G=
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ENSP00000478114.2:p.Ser1861=
|
|
ENST00000634433.2:c.5459G=
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ENSP00000489431.2:p.Ser1820=
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ENST00000644379.2:c.5648G=
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ENSP00000496570.2:p.Ser1883=
|
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ENST00000644555.2:c.2132G=
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ENSP00000494614.2:p.Ser711=
|
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ENST00000652672.2:c.5441G=
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ENSP00000498906.2:p.Ser1814=
|
|
ENST00000484087.6:c.2144G=
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ENSP00000419481.2:p.Ser715=
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ENST00000700081.1:n.1465G=
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|
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ENST00000700082.1:n.946G=
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|
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ENST00000357654.9:c.5582G=
MANE Select
|
ENSP00000350283.3:p.Ser1861=
|
|
ENST00000471181.7:c.5645G=
|
ENSP00000418960.2:p.Ser1882=
|
|
ENST00000644379.1:c.1969G=
|
|
|
ENST00000352993.7:c.2156G=
|
ENSP00000312236.5:p.Ser719=
|
|
ENST00000357654.7:c.5582G=
|
ENSP00000350283.3:p.Ser1861=
|
|
ENST00000461221.5:c.*5365G=
|
ENSP00000418548.1:n.*5365G=
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|
ENST00000468300.5:c.*96G=
|
ENSP00000417148.1:n.*96G=
|
|
ENST00000471181.6:c.5645G=
|
ENSP00000418960.2:p.Ser1882=
|
|
ENST00000491747.6:c.2270G=
|
ENSP00000420705.2:p.Ser757=
|
|
ENST00000493795.5:c.5441G=
|
ENSP00000418775.1:p.Ser1814=
|
|
ENST00000586385.5:c.512G=
|
ENSP00000465818.1:p.Ser171=
|
|
ENST00000591534.5:c.1055G=
|
ENSP00000467329.1:p.Ser352=
|
|
ENST00000591849.5:c.281G=
|
ENSP00000465347.1:p.Ser94=
|
|
NM_007294.3:c.5582G= , LRG_292t1:c.5582G=
|
NP_009225.1:p.Ser1861=
|
|
NM_007297.3:c.5441G=
|
NP_009228.2:p.Ser1814=
|
|
NM_007298.3:c.2270G=
|
NP_009229.2:p.Ser757=
|
|
NM_007299.3:c.*96G=
|
NP_009230.2:n.*96G=
|
|
NM_007300.3:c.5645G=
|
NP_009231.2:p.Ser1882=
|
|
NR_027676.1:n.5718G=
|
|
|
NM_007294.4:c.5582G=
MANE Select
|
NP_009225.1:p.Ser1861=
|
|
NM_007297.4:c.5441G=
|
NP_009228.2:p.Ser1814=
|
|
NM_007299.4:c.*96G=
|
NP_009230.2:n.*96G=
|
|
NM_007300.4:c.5645G=
|
NP_009231.2:p.Ser1882=
|
|
NR_027676.2:n.5759G=
|
|
|