ENST00000375128.5:c.822A>C
MANE Select
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ENSP00000364270.5:p.Ter274Cys
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ENST00000375128.4:c.822A>C
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ENSP00000364270.4:p.Ter274Cys
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ENST00000462523.5:c.*258A>C
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ENSP00000433006.1:n.*258A>C
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ENST00000485042.1:n.334A>C
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NM_000380.3:c.822A>C , LRG_471t1:c.822A>C
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NP_000371.1:p.Ter274Cys
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NR_027302.1:n.1170A>C
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XM_006717278.1:c.772+50A>C
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XP_006717341.1:n.772+50A>C
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XM_011518988.1:c.772+50A>C
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XP_011517290.1:n.772+50A>C
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NM_001354975.1:c.696A>C
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NP_001341904.1:p.Ter232Cys
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NR_149091.1:n.667A>C
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NR_149092.1:n.833A>C
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NR_149093.1:n.1359A>C
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|
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NR_149094.1:n.1253A>C
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|
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NM_000380.4:c.822A>C
MANE Select
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NP_000371.1:p.Ter274Cys
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NM_001354975.2:c.696A>C
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NP_001341904.1:p.Ter232Cys
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NR_027302.2:n.1101A>C
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NR_149091.2:n.598A>C
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NR_149092.2:n.764A>C
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NR_149093.2:n.1290A>C
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NR_149094.2:n.1184A>C
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