ENST00000461574.2:c.5438C>T
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ENSP00000417241.2:p.Ala1813Val
|
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ENST00000470026.6:c.5441C>T
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ENSP00000419274.2:p.Ala1814Val
|
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ENST00000473961.6:c.5315C>T
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ENSP00000420201.2:p.Ala1772Val
|
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ENST00000476777.6:c.5435C>T
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ENSP00000417554.2:p.Ala1812Val
|
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ENST00000477152.6:c.5363C>T
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ENSP00000419988.2:p.Ala1788Val
|
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ENST00000478531.6:c.2129C>T
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ENSP00000420412.2:p.Ala710Val
|
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ENST00000489037.2:c.5363C>T
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ENSP00000420781.2:p.Ala1788Val
|
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ENST00000493919.6:c.1991C>T
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ENSP00000418819.2:p.Ala664Val
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ENST00000494123.6:c.5441C>T
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ENSP00000419103.2:p.Ala1814Val
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ENST00000497488.2:c.4553C>T
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ENSP00000418986.2:p.Ala1518Val
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ENST00000618469.2:c.5441C>T
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ENSP00000478114.2:p.Ala1814Val
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ENST00000634433.2:c.5318C>T
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ENSP00000489431.2:p.Ala1773Val
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ENST00000644379.2:c.5507C>T
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ENSP00000496570.2:p.Ala1836Val
|
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ENST00000644555.2:c.1991C>T
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ENSP00000494614.2:p.Ala664Val
|
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ENST00000652672.2:c.5300C>T
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ENSP00000498906.2:p.Ala1767Val
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ENST00000484087.6:c.2003C>T
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ENSP00000419481.2:p.Ala668Val
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ENST00000700081.1:n.1324C>T
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|
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ENST00000700082.1:n.805C>T
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|
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ENST00000357654.9:c.5441C>T
MANE Select
|
ENSP00000350283.3:p.Ala1814Val
|
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ENST00000471181.7:c.5504C>T
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ENSP00000418960.2:p.Ala1835Val
|
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ENST00000644379.1:c.1828C>T
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|
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ENST00000352993.7:c.2015C>T
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ENSP00000312236.5:p.Ala672Val
|
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ENST00000357654.7:c.5441C>T
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ENSP00000350283.3:p.Ala1814Val
|
|
ENST00000461221.5:c.*5224C>T
|
ENSP00000418548.1:n.*5224C>T
|
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ENST00000468300.5:c.2055C>T
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ENSP00000417148.1:p.Cys685=
|
|
ENST00000471181.6:c.5504C>T
|
ENSP00000418960.2:p.Ala1835Val
|
|
ENST00000491747.6:c.2129C>T
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ENSP00000420705.2:p.Ala710Val
|
|
ENST00000493795.5:c.5300C>T
|
ENSP00000418775.1:p.Ala1767Val
|
|
ENST00000586385.5:c.371C>T
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ENSP00000465818.1:p.Ala124Val
|
|
ENST00000591534.5:c.914C>T
|
ENSP00000467329.1:p.Ala305Val
|
|
ENST00000591849.5:c.140C>T
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ENSP00000465347.1:p.Ala47Val
|
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NM_007294.3:c.5441C>T , LRG_292t1:c.5441C>T
|
NP_009225.1:p.Ala1814Val
|
|
NM_007297.3:c.5300C>T
|
NP_009228.2:p.Ala1767Val
|
|
NM_007298.3:c.2129C>T
|
NP_009229.2:p.Ala710Val
|
|
NM_007299.3:c.2055C>T
|
NP_009230.2:p.Cys685=
|
|
NM_007300.3:c.5504C>T
|
NP_009231.2:p.Ala1835Val
|
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NR_027676.1:n.5577C>T
|
|
|
NM_007294.4:c.5441C>T
MANE Select
|
NP_009225.1:p.Ala1814Val
|
|
NM_007297.4:c.5300C>T
|
NP_009228.2:p.Ala1767Val
|
|
NM_007299.4:c.2055C>T
|
NP_009230.2:p.Cys685=
|
|
NM_007300.4:c.5504C>T
|
NP_009231.2:p.Ala1835Val
|
|
NR_027676.2:n.5618C>T
|
|
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