ENST00000480188.2:n.1512T>G
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ENST00000696279.1:c.4798T>G
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ENST00000696280.1:n.4567T>G
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|
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ENST00000696281.1:c.4496T>G
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ENSP00000512521.1:p.Phe1499Cys
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ENST00000697921.1:n.3356T>G
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ENST00000697922.1:c.*4468T>G
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ENSP00000513478.1:n.*4468T>G
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ENST00000697923.1:n.4923T>G
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ENST00000223642.3:c.4478T>G
MANE Select
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ENSP00000223642.1:p.Phe1493Cys
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ENST00000223642.2:c.4478T>G
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ENSP00000223642.1:p.Phe1493Cys
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ENST00000480188.1:n.11T>G
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NM_001735.2:c.4478T>G , LRG_28t1:c.4478T>G
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NP_001726.2:p.Phe1493Cys
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XM_011518980.1:c.4493T>G
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XP_011517282.1:p.Phe1498Cys
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NM_001317163.1:c.4496T>G
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NP_001304092.1:p.Phe1499Cys
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NM_001317163.2:c.4496T>G
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NP_001304092.1:p.Phe1499Cys
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NM_001735.3:c.4478T>G
MANE Select
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NP_001726.2:p.Phe1493Cys
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