ENST00000339077.10:c.1120A>G
MANE Select
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ENSP00000343273.4:p.Ser374Gly
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ENST00000339077.9:c.1120A>G
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ENSP00000343273.4:p.Ser374Gly
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ENST00000409689.5:c.976A>G
|
ENSP00000386263.1:p.Ser326Gly
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ENST00000469576.1:n.7A>G
|
|
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ENST00000521082.5:c.*1128A>G
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ENSP00000430351.1:n.*1128A>G
|
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NM_001031710.2:c.1120A>G
|
NP_001026880.2:p.Ser374Gly
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NM_018846.4:c.976A>G
|
NP_061334.4:p.Ser326Gly
|
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NR_033328.1:n.1544A>G
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XM_006715753.1:c.1159A>G
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XP_006715816.1:p.Ser387Gly
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XM_006715754.1:c.1093A>G
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XP_006715817.1:p.Ser365Gly
|
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XM_006715755.1:c.1093A>G
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XP_006715818.1:p.Ser365Gly
|
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XM_006715756.1:c.1015A>G
|
XP_006715819.1:p.Ser339Gly
|
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XM_006715753.3:c.1159A>G
|
XP_006715816.1:p.Ser387Gly
|
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XM_006715754.3:c.1093A>G
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XP_006715817.1:p.Ser365Gly
|
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XM_006715755.3:c.1093A>G
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XP_006715818.1:p.Ser365Gly
|
|
XM_006715756.3:c.1015A>G
|
XP_006715819.1:p.Ser339Gly
|
|
XM_017012439.2:c.1054A>G
|
XP_016867928.1:p.Ser352Gly
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NM_001031710.3:c.1120A>G
MANE Select
|
NP_001026880.2:p.Ser374Gly
|
|
NM_018846.5:c.976A>G
|
NP_061334.4:p.Ser326Gly
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NR_033328.2:n.1493A>G
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