ENST00000367698.4:c.1271G>T
MANE Select
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ENSP00000356671.3:p.Gly424Val
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ENST00000367698.3:c.1271G>T
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ENSP00000356671.3:p.Gly424Val
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ENST00000617423.4:c.656G>T
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ENSP00000478688.1:p.Gly219Val
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NM_000488.3:c.1271G>T , LRG_577t1:c.1271G>T
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NP_000479.1:p.Gly424Val
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XM_005245198.2:c.1127G>T
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XP_005245255.1:p.Gly376Val
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NM_001365052.1:c.1127G>T
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NP_001351981.1:p.Gly376Val
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NM_000488.4:c.1271G>T
MANE Select
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NP_000479.1:p.Gly424Val
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NM_001365052.2:c.1127G>T
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NP_001351981.1:p.Gly376Val
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NM_001386302.1:c.1394G>T
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NP_001373231.1:p.Gly465Val
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NM_001386303.1:c.1352G>T
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NP_001373232.1:p.Gly451Val
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NM_001386304.1:c.1250G>T
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NP_001373233.1:p.Gly417Val
|
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NM_001386305.1:c.1214G>T
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NP_001373234.1:p.Gly405Val
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NM_001386306.1:c.1055G>T
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NP_001373235.1:p.Gly352Val
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