ENST00000450114.7:c.1432G>T
MANE Select
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ENSP00000402084.2:p.Gly478Cys
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ENST00000530712.6:c.250G>T
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ENSP00000434148.2:p.Gly84Cys
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ENST00000680141.1:c.*382G>T
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ENSP00000506686.1:n.*382G>T
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ENST00000681684.1:c.790G>T
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ENSP00000506667.1:p.Gly264Cys
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ENST00000299613.10:c.790G>T
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ENSP00000299613.5:p.Gly264Cys
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ENST00000450114.6:c.1432G>T
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ENSP00000402084.2:p.Gly478Cys
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ENST00000524612.5:c.316G>T
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ENSP00000434446.1:p.Gly106Cys
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ENST00000530175.5:c.279G>T
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ENST00000530712.5:c.250G>T
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ENSP00000434148.1:p.Gly84Cys
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ENST00000532275.1:n.219G>T
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|
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NM_001143976.1:c.790G>T
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NP_001137448.1:p.Gly264Cys
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NM_003390.3:c.1432G>T
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NP_003381.1:p.Gly478Cys
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XM_005253118.3:c.1432G>T
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XP_005253175.1:p.Gly478Cys
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XM_005253119.3:c.790G>T
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XP_005253176.1:p.Gly264Cys
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NM_003390.4:c.1432G>T
MANE Select
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NP_003381.1:p.Gly478Cys
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NM_001143976.2:c.790G>T
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NP_001137448.1:p.Gly264Cys
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