ENST00000367698.4:c.842C>T
MANE Select
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ENSP00000356671.3:p.Ala281Val
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ENST00000367698.3:c.842C>T
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ENSP00000356671.3:p.Ala281Val
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ENST00000487183.1:n.493C>T
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ENST00000617423.4:c.559+2001C>T
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ENSP00000478688.1:n.559+2001C>T
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NM_000488.3:c.842C>T , LRG_577t1:c.842C>T
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NP_000479.1:p.Ala281Val
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XM_005245198.2:c.698C>T
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XP_005245255.1:p.Ala233Val
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NM_001365052.1:c.698C>T
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NP_001351981.1:p.Ala233Val
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NM_000488.4:c.842C>T
MANE Select
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NP_000479.1:p.Ala281Val
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NM_001365052.2:c.698C>T
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NP_001351981.1:p.Ala233Val
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NM_001386302.1:c.965C>T
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NP_001373231.1:p.Ala322Val
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NM_001386303.1:c.923C>T
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NP_001373232.1:p.Ala308Val
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NM_001386304.1:c.821C>T
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NP_001373233.1:p.Ala274Val
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NM_001386305.1:c.785C>T
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NP_001373234.1:p.Ala262Val
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NM_001386306.1:c.626C>T
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NP_001373235.1:p.Ala209Val
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