ENST00000442544.7:c.494G>T
MANE Select
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ENSP00000389140.2:p.Gly165Val
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ENST00000304775.12:c.295G>T
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ENST00000412726.5:c.425G>T
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ENSP00000397322.2:p.Gly142Val
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ENST00000442544.6:c.494G>T
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ENSP00000389140.2:p.Gly165Val
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ENST00000579349.1:c.415G>T
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ENST00000580024.1:n.407G>T
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ENST00000581559.1:c.415G>T
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ENSP00000463463.1:n.415G>T
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NM_005215.3:c.494G>T
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NP_005206.2:p.Gly165Val
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XM_011525843.1:c.494G>T
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XP_011524145.1:p.Gly165Val
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XM_011525845.1:c.494G>T
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XP_011524147.1:p.Gly165Val
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XM_011525846.1:c.494G>T
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XP_011524148.1:p.Gly165Val
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XM_017025568.1:c.494G>T
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XP_016881057.1:p.Gly165Val
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XM_017025569.1:c.494G>T
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XP_016881058.1:p.Gly165Val
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NM_005215.4:c.494G>T
MANE Select
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NP_005206.2:p.Gly165Val
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