ENST00000270357.10:c.1555G>T
MANE Select
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ENSP00000270357.4:p.Ala519Ser
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ENST00000270357.8:c.862G>T
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ENSP00000270357.3:p.Ala288Ser
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ENST00000437406.1:c.121G>T
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ENSP00000403319.1:p.Ala41Ser
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ENST00000451363.5:c.196G>T
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ENSP00000414661.1:p.Ala66Ser
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ENST00000464550.5:n.391G>T
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ENST00000471657.1:n.358G>T
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ENST00000481757.5:n.2489G>T
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ENST00000486058.5:n.1668G>T
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ENST00000493398.5:n.701G>T
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NM_018226.4:c.1555G>T
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NP_060696.4:p.Ala519Ser
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XM_005247036.3:c.1522G>T
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XP_005247093.1:p.Ala508Ser
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NM_018226.5:c.1555G>T
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NP_060696.4:p.Ala519Ser
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XM_005247036.4:c.1522G>T
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XP_005247093.1:p.Ala508Ser
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NM_018226.6:c.1555G>T
MANE Select
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NP_060696.4:p.Ala519Ser
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