ENST00000339077.10:c.1004A>G
MANE Select
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ENSP00000343273.4:p.Asp335Gly
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ENST00000339077.9:c.1004A>G
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ENSP00000343273.4:p.Asp335Gly
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ENST00000409689.5:c.860A>G
|
ENSP00000386263.1:p.Asp287Gly
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ENST00000521082.5:c.*1012A>G
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ENSP00000430351.1:n.*1012A>G
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NM_001031710.2:c.1004A>G
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NP_001026880.2:p.Asp335Gly
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NM_018846.4:c.860A>G
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NP_061334.4:p.Asp287Gly
|
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NR_033328.1:n.1428A>G
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|
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XM_006715753.1:c.1043A>G
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XP_006715816.1:p.Asp348Gly
|
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XM_006715754.1:c.977A>G
|
XP_006715817.1:p.Asp326Gly
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XM_006715755.1:c.977A>G
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XP_006715818.1:p.Asp326Gly
|
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XM_006715756.1:c.899A>G
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XP_006715819.1:p.Asp300Gly
|
|
XM_006715753.3:c.1043A>G
|
XP_006715816.1:p.Asp348Gly
|
|
XM_006715754.3:c.977A>G
|
XP_006715817.1:p.Asp326Gly
|
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XM_006715755.3:c.977A>G
|
XP_006715818.1:p.Asp326Gly
|
|
XM_006715756.3:c.899A>G
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XP_006715819.1:p.Asp300Gly
|
|
XM_017012439.2:c.938A>G
|
XP_016867928.1:p.Asp313Gly
|
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NM_001031710.3:c.1004A>G
MANE Select
|
NP_001026880.2:p.Asp335Gly
|
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NM_018846.5:c.860A>G
|
NP_061334.4:p.Asp287Gly
|
|
NR_033328.2:n.1377A>G
|
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