ENST00000367698.4:c.827G>T
MANE Select
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ENSP00000356671.3:p.Gly276Val
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ENST00000367698.3:c.827G>T
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ENSP00000356671.3:p.Gly276Val
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ENST00000487183.1:n.478G>T
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ENST00000617423.4:c.559+1986G>T
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ENSP00000478688.1:n.559+1986G>T
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NM_000488.3:c.827G>T , LRG_577t1:c.827G>T
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NP_000479.1:p.Gly276Val
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XM_005245198.2:c.683G>T
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XP_005245255.1:p.Gly228Val
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NM_001365052.1:c.683G>T
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NP_001351981.1:p.Gly228Val
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NM_000488.4:c.827G>T
MANE Select
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NP_000479.1:p.Gly276Val
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NM_001365052.2:c.683G>T
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NP_001351981.1:p.Gly228Val
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NM_001386302.1:c.950G>T
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NP_001373231.1:p.Gly317Val
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NM_001386303.1:c.908G>T
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NP_001373232.1:p.Gly303Val
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NM_001386304.1:c.806G>T
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NP_001373233.1:p.Gly269Val
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NM_001386305.1:c.770G>T
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NP_001373234.1:p.Gly257Val
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NM_001386306.1:c.611G>T
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NP_001373235.1:p.Gly204Val
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