ENST00000461574.2:c.4878A>C
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ENSP00000417241.2:p.Ala1626=
|
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ENST00000470026.6:c.4881A>C
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ENSP00000419274.2:p.Ala1627=
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ENST00000473961.6:c.4755A>C
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ENSP00000420201.2:p.Ala1585=
|
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ENST00000476777.6:c.4875A>C
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ENSP00000417554.2:p.Ala1625=
|
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ENST00000477152.6:c.4803A>C
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ENSP00000419988.2:p.Ala1601=
|
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ENST00000478531.6:c.1569A>C
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ENSP00000420412.2:p.Ala523=
|
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ENST00000489037.2:c.4803A>C
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ENSP00000420781.2:p.Ala1601=
|
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ENST00000493919.6:c.1431A>C
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ENSP00000418819.2:p.Ala477=
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ENST00000494123.6:c.4881A>C
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ENSP00000419103.2:p.Ala1627=
|
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ENST00000497488.2:c.3993A>C
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ENSP00000418986.2:p.Ala1331=
|
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ENST00000618469.2:c.4881A>C
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ENSP00000478114.2:p.Ala1627=
|
|
ENST00000634433.2:c.4758A>C
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ENSP00000489431.2:p.Ala1586=
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ENST00000644379.2:c.4947A>C
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ENSP00000496570.2:p.Ala1649=
|
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ENST00000644555.2:c.1431A>C
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ENSP00000494614.2:p.Ala477=
|
|
ENST00000652672.2:c.4740A>C
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ENSP00000498906.2:p.Ala1580=
|
|
ENST00000484087.6:c.1443A>C
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ENSP00000419481.2:p.Ala481=
|
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ENST00000700182.1:c.1488A>C
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ENSP00000514849.1:p.Ala496=
|
|
ENST00000357654.9:c.4881A>C
MANE Select
|
ENSP00000350283.3:p.Ala1627=
|
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ENST00000471181.7:c.4944A>C
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ENSP00000418960.2:p.Ala1648=
|
|
ENST00000644379.1:c.1268A>C
|
|
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ENST00000352993.7:c.1455A>C
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ENSP00000312236.5:p.Ala485=
|
|
ENST00000357654.7:c.4881A>C
|
ENSP00000350283.3:p.Ala1627=
|
|
ENST00000461221.5:c.*4664A>C
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ENSP00000418548.1:n.*4664A>C
|
|
ENST00000468300.5:c.1569A>C
|
ENSP00000417148.1:p.Ala523=
|
|
ENST00000471181.6:c.4944A>C
|
ENSP00000418960.2:p.Ala1648=
|
|
ENST00000472490.1:n.34A>C
|
|
|
ENST00000478531.5:c.1569A>C
|
ENSP00000420412.1:p.Ala523=
|
|
ENST00000484087.5:c.1194A>C
|
ENSP00000419481.1:p.Ala398=
|
|
ENST00000491747.6:c.1569A>C
|
ENSP00000420705.2:p.Ala523=
|
|
ENST00000493795.5:c.4740A>C
|
ENSP00000418775.1:p.Ala1580=
|
|
ENST00000493919.5:c.1431A>C
|
ENSP00000418819.1:p.Ala477=
|
|
ENST00000586385.5:c.5-7082A>C
|
ENSP00000465818.1:n.5-7082A>C
|
|
ENST00000591534.5:c.354A>C
|
ENSP00000467329.1:p.Ala118=
|
|
ENST00000591849.5:c.-98-20843A>C
|
ENSP00000465347.1:n.-98-20843A>C
|
|
NM_007294.3:c.4881A>C , LRG_292t1:c.4881A>C
|
NP_009225.1:p.Ala1627=
|
|
NM_007297.3:c.4740A>C
|
NP_009228.2:p.Ala1580=
|
|
NM_007298.3:c.1569A>C
|
NP_009229.2:p.Ala523=
|
|
NM_007299.3:c.1569A>C
|
NP_009230.2:p.Ala523=
|
|
NM_007300.3:c.4944A>C
|
NP_009231.2:p.Ala1648=
|
|
NR_027676.1:n.5017A>C
|
|
|
NM_007294.4:c.4881A>C
MANE Select
|
NP_009225.1:p.Ala1627=
|
|
NM_007297.4:c.4740A>C
|
NP_009228.2:p.Ala1580=
|
|
NM_007299.4:c.1569A>C
|
NP_009230.2:p.Ala523=
|
|
NM_007300.4:c.4944A>C
|
NP_009231.2:p.Ala1648=
|
|
NR_027676.2:n.5058A>C
|
|
|