ENST00000225964.10:c.982A>G
MANE Select
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ENSP00000225964.6:p.Thr328Ala
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ENST00000225964.9:c.982A>G
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ENSP00000225964.5:p.Thr328Ala
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ENST00000485870.1:n.307A>G
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NM_000088.3:c.982A>G , LRG_1t1:c.982A>G
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NP_000079.2:p.Thr328Ala
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XM_005257058.3:c.982A>G
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XP_005257115.2:p.Thr328Ala
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XM_005257059.3:c.957+139A>G
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XP_005257116.2:n.957+139A>G
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XM_011524341.1:c.957+139A>G
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XP_011522643.1:n.957+139A>G
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XM_005257058.4:c.982A>G
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XP_005257115.2:p.Thr328Ala
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XM_005257059.4:c.957+139A>G
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XP_005257116.2:n.957+139A>G
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NM_000088.4:c.982A>G
MANE Select
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NP_000079.2:p.Thr328Ala
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