ENST00000339077.10:c.1172A>G
MANE Select
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ENSP00000343273.4:p.Glu391Gly
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ENST00000339077.9:c.1172A>G
|
ENSP00000343273.4:p.Glu391Gly
|
|
ENST00000409689.5:c.1028A>G
|
ENSP00000386263.1:p.Glu343Gly
|
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ENST00000469576.1:n.59A>G
|
|
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ENST00000521082.5:c.*1180A>G
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ENSP00000430351.1:n.*1180A>G
|
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NM_001031710.2:c.1172A>G
|
NP_001026880.2:p.Glu391Gly
|
|
NM_018846.4:c.1028A>G
|
NP_061334.4:p.Glu343Gly
|
|
NR_033328.1:n.1596A>G
|
|
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XM_006715753.1:c.1211A>G
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XP_006715816.1:p.Glu404Gly
|
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XM_006715754.1:c.1145A>G
|
XP_006715817.1:p.Glu382Gly
|
|
XM_006715755.1:c.1145A>G
|
XP_006715818.1:p.Glu382Gly
|
|
XM_006715756.1:c.1067A>G
|
XP_006715819.1:p.Glu356Gly
|
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XM_006715753.3:c.1211A>G
|
XP_006715816.1:p.Glu404Gly
|
|
XM_006715754.3:c.1145A>G
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XP_006715817.1:p.Glu382Gly
|
|
XM_006715755.3:c.1145A>G
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XP_006715818.1:p.Glu382Gly
|
|
XM_006715756.3:c.1067A>G
|
XP_006715819.1:p.Glu356Gly
|
|
XM_017012439.2:c.1106A>G
|
XP_016867928.1:p.Glu369Gly
|
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NM_001031710.3:c.1172A>G
MANE Select
|
NP_001026880.2:p.Glu391Gly
|
|
NM_018846.5:c.1028A>G
|
NP_061334.4:p.Glu343Gly
|
|
NR_033328.2:n.1545A>G
|
|
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