ENST00000268053.11:c.1136C>T
MANE Select
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ENSP00000268053.6:p.Ala379Val
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ENST00000268053.10:c.1136C>T
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ENSP00000268053.6:p.Ala379Val
|
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ENST00000358632.8:c.662C>T
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ENSP00000351455.4:p.Ala221Val
|
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ENST00000435365.5:c.1136C>T
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ENSP00000391081.1:p.Ala379Val
|
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ENST00000566674.5:c.662C>T
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ENSP00000456941.1:p.Ala221Val
|
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NM_000781.2:c.1136C>T
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NP_000772.2:p.Ala379Val
|
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NM_001099773.1:c.662C>T
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NP_001093243.1:p.Ala221Val
|
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NM_000781.3:c.1136C>T
MANE Select
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NP_000772.2:p.Ala379Val
|
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NM_001099773.2:c.662C>T
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NP_001093243.1:p.Ala221Val
|
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