ENST00000225964.10:c.4124C>T
MANE Select
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ENSP00000225964.6:p.Ala1375Val
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ENST00000225964.9:c.4124C>T
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ENSP00000225964.5:p.Ala1375Val
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ENST00000510710.3:n.1089C>T
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NM_000088.3:c.4124C>T , LRG_1t1:c.4124C>T
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NP_000079.2:p.Ala1375Val
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XM_005257058.3:c.3854C>T
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XP_005257115.2:p.Ala1285Val
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XM_005257059.3:c.3206C>T
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XP_005257116.2:p.Ala1069Val
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XM_011524341.1:c.3926C>T
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XP_011522643.1:p.Ala1309Val
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XM_005257058.4:c.3854C>T
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XP_005257115.2:p.Ala1285Val
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XM_005257059.4:c.3206C>T
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XP_005257116.2:p.Ala1069Val
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NM_000088.4:c.4124C>T
MANE Select
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NP_000079.2:p.Ala1375Val
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