ENST00000339077.10:c.1027G>T
MANE Select
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ENSP00000343273.4:p.Gly343Cys
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ENST00000339077.9:c.1027G>T
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ENSP00000343273.4:p.Gly343Cys
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ENST00000409689.5:c.883G>T
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ENSP00000386263.1:p.Gly295Cys
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ENST00000521082.5:c.*1035G>T
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ENSP00000430351.1:n.*1035G>T
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NM_001031710.2:c.1027G>T
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NP_001026880.2:p.Gly343Cys
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NM_018846.4:c.883G>T
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NP_061334.4:p.Gly295Cys
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NR_033328.1:n.1451G>T
|
|
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XM_006715753.1:c.1066G>T
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XP_006715816.1:p.Gly356Cys
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XM_006715754.1:c.1000G>T
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XP_006715817.1:p.Gly334Cys
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XM_006715755.1:c.1000G>T
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XP_006715818.1:p.Gly334Cys
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XM_006715756.1:c.922G>T
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XP_006715819.1:p.Gly308Cys
|
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XM_006715753.3:c.1066G>T
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XP_006715816.1:p.Gly356Cys
|
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XM_006715754.3:c.1000G>T
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XP_006715817.1:p.Gly334Cys
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XM_006715755.3:c.1000G>T
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XP_006715818.1:p.Gly334Cys
|
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XM_006715756.3:c.922G>T
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XP_006715819.1:p.Gly308Cys
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XM_017012439.2:c.961G>T
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XP_016867928.1:p.Gly321Cys
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NM_001031710.3:c.1027G>T
MANE Select
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NP_001026880.2:p.Gly343Cys
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NM_018846.5:c.883G>T
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NP_061334.4:p.Gly295Cys
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NR_033328.2:n.1400G>T
|
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