ENST00000211998.10:c.2751C>A
MANE Select
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ENSP00000211998.5:p.Gly917=
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ENST00000211998.8:c.2751C>A
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ENSP00000211998.4:p.Gly917=
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ENST00000372755.7:c.2746-2270C>A
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ENSP00000361841.3:n.2746-2270C>A
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ENST00000436396.1:c.1767C>A
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ENSP00000415489.1:p.Gly589=
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ENST00000623461.3:n.5549-2270C>A
|
|
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ENST00000624354.3:c.*2506C>A
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ENSP00000485551.1:n.*2506C>A
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NM_003373.3:c.2746-2270C>A
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NP_003364.1:n.2746-2270C>A
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NM_014000.2:c.2751C>A , LRG_383t1:c.2751C>A
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NP_054706.1:p.Gly917=
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XM_005270142.1:c.2754C>A
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XP_005270199.1:p.Gly918=
|
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XM_005270143.1:c.2749-2270C>A
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XP_005270200.1:n.2749-2270C>A
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NM_003373.4:c.2746-2270C>A
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NP_003364.1:n.2746-2270C>A
|
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NM_014000.3:c.2751C>A
MANE Select
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NP_054706.1:p.Gly917=
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