ENST00000339077.10:c.1024G>T
MANE Select
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ENSP00000343273.4:p.Gly342Ter
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ENST00000339077.9:c.1024G>T
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ENSP00000343273.4:p.Gly342Ter
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ENST00000409689.5:c.880G>T
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ENSP00000386263.1:p.Gly294Ter
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ENST00000521082.5:c.*1032G>T
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ENSP00000430351.1:n.*1032G>T
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NM_001031710.2:c.1024G>T
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NP_001026880.2:p.Gly342Ter
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NM_018846.4:c.880G>T
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NP_061334.4:p.Gly294Ter
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NR_033328.1:n.1448G>T
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XM_006715753.1:c.1063G>T
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XP_006715816.1:p.Gly355Ter
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XM_006715754.1:c.997G>T
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XP_006715817.1:p.Gly333Ter
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XM_006715755.1:c.997G>T
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XP_006715818.1:p.Gly333Ter
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XM_006715756.1:c.919G>T
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XP_006715819.1:p.Gly307Ter
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XM_006715753.3:c.1063G>T
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XP_006715816.1:p.Gly355Ter
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XM_006715754.3:c.997G>T
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XP_006715817.1:p.Gly333Ter
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XM_006715755.3:c.997G>T
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XP_006715818.1:p.Gly333Ter
|
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XM_006715756.3:c.919G>T
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XP_006715819.1:p.Gly307Ter
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XM_017012439.2:c.958G>T
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XP_016867928.1:p.Gly320Ter
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NM_001031710.3:c.1024G>T
MANE Select
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NP_001026880.2:p.Gly342Ter
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NM_018846.5:c.880G>T
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NP_061334.4:p.Gly294Ter
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NR_033328.2:n.1397G>T
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