ENST00000225964.10:c.3227G>T
MANE Select
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ENSP00000225964.6:p.Gly1076Val
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ENST00000225964.9:c.3227G>T
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ENSP00000225964.5:p.Gly1076Val
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ENST00000486572.1:n.425G>T
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ENST00000511732.1:n.551G>T
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NM_000088.3:c.3227G>T , LRG_1t1:c.3227G>T
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NP_000079.2:p.Gly1076Val
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XM_005257058.3:c.2957G>T
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XP_005257115.2:p.Gly986Val
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XM_005257059.3:c.2309G>T
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XP_005257116.2:p.Gly770Val
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XM_011524341.1:c.3029G>T
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XP_011522643.1:p.Gly1010Val
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XM_005257058.4:c.2957G>T
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XP_005257115.2:p.Gly986Val
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XM_005257059.4:c.2309G>T
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XP_005257116.2:p.Gly770Val
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NM_000088.4:c.3227G>T
MANE Select
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NP_000079.2:p.Gly1076Val
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