ENST00000270357.10:c.1626A>T
MANE Select
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ENSP00000270357.4:p.Ala542=
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ENST00000270357.8:c.933A>T
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ENSP00000270357.3:p.Ala311=
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ENST00000437406.1:c.192A>T
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ENSP00000403319.1:p.Ala64=
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ENST00000451363.5:c.267A>T
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ENSP00000414661.1:p.Ala89=
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ENST00000464550.5:n.462A>T
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ENST00000471657.1:n.429A>T
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ENST00000481757.5:n.2560A>T
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ENST00000486058.5:n.1739A>T
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ENST00000493398.5:n.772A>T
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NM_018226.4:c.1626A>T
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NP_060696.4:p.Ala542=
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XM_005247036.3:c.1593A>T
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XP_005247093.1:p.Ala531=
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NM_018226.5:c.1626A>T
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NP_060696.4:p.Ala542=
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XM_005247036.4:c.1593A>T
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XP_005247093.1:p.Ala531=
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NM_018226.6:c.1626A>T
MANE Select
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NP_060696.4:p.Ala542=
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