ENST00000461574.2:c.4357G=
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ENSP00000417241.2:p.Val1453=
|
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ENST00000470026.6:c.4357G=
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ENSP00000419274.2:p.Ala1453=
|
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ENST00000473961.6:c.4231G=
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ENSP00000420201.2:p.Ala1411=
|
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ENST00000476777.6:c.4351G=
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ENSP00000417554.2:p.Ala1451=
|
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ENST00000477152.6:c.4279G=
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ENSP00000419988.2:p.Ala1427=
|
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ENST00000478531.6:c.1045G=
|
ENSP00000420412.2:p.Ala349=
|
|
ENST00000489037.2:c.4279G=
|
ENSP00000420781.2:p.Ala1427=
|
|
ENST00000493919.6:c.907G=
|
ENSP00000418819.2:p.Ala303=
|
|
ENST00000494123.6:c.4357G=
|
ENSP00000419103.2:p.Ala1453=
|
|
ENST00000497488.2:c.3469G=
|
ENSP00000418986.2:p.Ala1157=
|
|
ENST00000618469.2:c.4357G=
|
ENSP00000478114.2:p.Ala1453=
|
|
ENST00000634433.2:c.4234G=
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ENSP00000489431.2:p.Ala1412=
|
|
ENST00000644379.2:c.4357G=
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ENSP00000496570.2:p.Asp1453=
|
|
ENST00000644555.2:c.907G=
|
ENSP00000494614.2:p.Ala303=
|
|
ENST00000652672.2:c.4216G=
|
ENSP00000498906.2:p.Ala1406=
|
|
ENST00000484087.6:c.922G=
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ENSP00000419481.2:p.Val308=
|
|
ENST00000700182.1:c.967G=
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ENSP00000514849.1:p.Val323=
|
|
ENST00000357654.9:c.4357G=
MANE Select
|
ENSP00000350283.3:p.Ala1453=
|
|
ENST00000471181.7:c.4357G=
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ENSP00000418960.2:p.Asp1453=
|
|
ENST00000644379.1:c.678G=
|
|
|
ENST00000352993.7:c.931G=
|
ENSP00000312236.5:p.Ala311=
|
|
ENST00000357654.7:c.4357G=
|
ENSP00000350283.3:p.Ala1453=
|
|
ENST00000461221.5:c.*4140G=
|
ENSP00000418548.1:n.*4140G=
|
|
ENST00000461574.1:c.651G=
|
|
|
ENST00000468300.5:c.1048G=
|
ENSP00000417148.1:p.Val350=
|
|
ENST00000471181.6:c.4357G=
|
ENSP00000418960.2:p.Asp1453=
|
|
ENST00000478531.5:c.1045G=
|
ENSP00000420412.1:p.Ala349=
|
|
ENST00000484087.5:c.670G=
|
ENSP00000419481.1:p.Ala224=
|
|
ENST00000487825.5:c.673G=
|
ENSP00000418212.1:p.Ala225=
|
|
ENST00000491747.6:c.1048G=
|
ENSP00000420705.2:p.Val350=
|
|
ENST00000493795.5:c.4216G=
|
ENSP00000418775.1:p.Ala1406=
|
|
ENST00000493919.5:c.907G=
|
ENSP00000418819.1:p.Ala303=
|
|
ENST00000586385.5:c.5-18453G=
|
ENSP00000465818.1:n.5-18453G=
|
|
ENST00000591534.5:c.-43-7883G=
|
ENSP00000467329.1:n.-43-7883G=
|
|
ENST00000591849.5:c.-98-32214G=
|
ENSP00000465347.1:n.-98-32214G=
|
|
ENST00000621897.1:n.251G=
|
|
|
NM_007294.3:c.4357G= , LRG_292t1:c.4357G=
|
NP_009225.1:p.Ala1453=
|
|
NM_007297.3:c.4216G=
|
NP_009228.2:p.Ala1406=
|
|
NM_007298.3:c.1048G=
|
NP_009229.2:p.Val350=
|
|
NM_007299.3:c.1048G=
|
NP_009230.2:p.Val350=
|
|
NM_007300.3:c.4357G=
|
NP_009231.2:p.Asp1453=
|
|
NR_027676.1:n.4493G=
|
|
|
NM_007294.4:c.4357G=
MANE Select
|
NP_009225.1:p.Ala1453=
|
|
NM_007297.4:c.4216G=
|
NP_009228.2:p.Ala1406=
|
|
NM_007299.4:c.1048G=
|
NP_009230.2:p.Val350=
|
|
NM_007300.4:c.4357G=
|
NP_009231.2:p.Asp1453=
|
|
NR_027676.2:n.4534G=
|
|
|