ENST00000270357.10:c.1642G>T
MANE Select
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ENSP00000270357.4:p.Ala548Ser
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ENST00000270357.8:c.949G>T
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ENSP00000270357.3:p.Ala317Ser
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ENST00000437406.1:c.208G>T
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ENSP00000403319.1:p.Ala70Ser
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ENST00000451363.5:c.283G>T
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ENSP00000414661.1:p.Ala95Ser
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ENST00000464550.5:n.478G>T
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ENST00000471657.1:n.445G>T
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ENST00000481757.5:n.2576G>T
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ENST00000486058.5:n.1755G>T
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ENST00000493398.5:n.788G>T
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NM_018226.4:c.1642G>T
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NP_060696.4:p.Ala548Ser
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XM_005247036.3:c.1609G>T
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XP_005247093.1:p.Ala537Ser
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NM_018226.5:c.1642G>T
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NP_060696.4:p.Ala548Ser
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XM_005247036.4:c.1609G>T
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XP_005247093.1:p.Ala537Ser
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NM_018226.6:c.1642G>T
MANE Select
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NP_060696.4:p.Ala548Ser
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