ENST00000339077.10:c.1081A>G
MANE Select
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ENSP00000343273.4:p.Ser361Gly
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ENST00000339077.9:c.1081A>G
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ENSP00000343273.4:p.Ser361Gly
|
|
ENST00000409689.5:c.937A>G
|
ENSP00000386263.1:p.Ser313Gly
|
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ENST00000521082.5:c.*1089A>G
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ENSP00000430351.1:n.*1089A>G
|
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NM_001031710.2:c.1081A>G
|
NP_001026880.2:p.Ser361Gly
|
|
NM_018846.4:c.937A>G
|
NP_061334.4:p.Ser313Gly
|
|
NR_033328.1:n.1505A>G
|
|
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XM_006715753.1:c.1120A>G
|
XP_006715816.1:p.Ser374Gly
|
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XM_006715754.1:c.1054A>G
|
XP_006715817.1:p.Ser352Gly
|
|
XM_006715755.1:c.1054A>G
|
XP_006715818.1:p.Ser352Gly
|
|
XM_006715756.1:c.976A>G
|
XP_006715819.1:p.Ser326Gly
|
|
XM_006715753.3:c.1120A>G
|
XP_006715816.1:p.Ser374Gly
|
|
XM_006715754.3:c.1054A>G
|
XP_006715817.1:p.Ser352Gly
|
|
XM_006715755.3:c.1054A>G
|
XP_006715818.1:p.Ser352Gly
|
|
XM_006715756.3:c.976A>G
|
XP_006715819.1:p.Ser326Gly
|
|
XM_017012439.2:c.1015A>G
|
XP_016867928.1:p.Ser339Gly
|
|
NM_001031710.3:c.1081A>G
MANE Select
|
NP_001026880.2:p.Ser361Gly
|
|
NM_018846.5:c.937A>G
|
NP_061334.4:p.Ser313Gly
|
|
NR_033328.2:n.1454A>G
|
|
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