ENST00000257290.10:c.1776A>G
MANE Select
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ENSP00000257290.5:p.Gly592=
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ENST00000257290.9:c.1776A>G
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ENSP00000257290.5:p.Gly592=
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ENST00000507166.5:c.1056A>G
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ENSP00000423325.1:p.Gly352=
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ENST00000509092.5:n.1594A>G
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ENST00000509490.5:c.1776A>G
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ENSP00000424218.1:p.Gly592=
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NM_006206.4:c.1776A>G , LRG_309t1:c.1776A>G
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NP_006197.1:p.Gly592=
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XM_005265743.1:c.1776A>G
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XP_005265800.1:p.Gly592=
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XM_006714039.2:c.1851A>G
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XP_006714102.1:p.Gly617=
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XM_006714041.2:c.1851A>G
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XP_006714104.1:p.Gly617=
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XM_011534385.1:c.1776A>G
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XP_011532687.1:p.Gly592=
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XM_011534386.1:c.1776A>G
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XP_011532688.1:p.Gly592=
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NM_001347827.1:c.1776A>G
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NP_001334756.1:p.Gly592=
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NM_001347828.1:c.1851A>G
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NP_001334757.1:p.Gly617=
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NM_001347829.1:c.1776A>G
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NP_001334758.1:p.Gly592=
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NM_001347830.1:c.1815A>G
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NP_001334759.1:p.Gly605=
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NM_006206.5:c.1776A>G
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NP_006197.1:p.Gly592=
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XM_006714041.3:c.1851A>G
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XP_006714104.1:p.Gly617=
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XM_017008281.1:c.1815A>G
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XP_016863770.1:p.Gly605=
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NM_006206.6:c.1776A>G
MANE Select
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NP_006197.1:p.Gly592=
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NM_001347827.2:c.1776A>G
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NP_001334756.1:p.Gly592=
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NM_001347828.2:c.1851A>G
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NP_001334757.1:p.Gly617=
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NM_001347829.2:c.1776A>G
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NP_001334758.1:p.Gly592=
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NM_001347830.2:c.1815A>G
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NP_001334759.1:p.Gly605=
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