ENST00000375128.5:c.751A>G
MANE Select
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ENSP00000364270.5:p.Asn251Asp
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ENST00000375128.4:c.751A>G
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ENSP00000364270.4:p.Asn251Asp
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ENST00000462523.5:c.*187A>G
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ENSP00000433006.1:n.*187A>G
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ENST00000485042.1:n.263A>G
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NM_000380.3:c.751A>G , LRG_471t1:c.751A>G
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NP_000371.1:p.Asn251Asp
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NR_027302.1:n.1099A>G
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XM_006717278.1:c.751A>G
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XP_006717341.1:p.Asn251Asp
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XM_011518988.1:c.751A>G
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XP_011517290.1:p.Asn251Asp
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XR_929839.1:n.1282A>G
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NM_001354975.1:c.625A>G
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NP_001341904.1:p.Asn209Asp
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NR_149091.1:n.596A>G
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NR_149092.1:n.762A>G
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NR_149093.1:n.1288A>G
|
|
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NR_149094.1:n.1182A>G
|
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NM_000380.4:c.751A>G
MANE Select
|
NP_000371.1:p.Asn251Asp
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NM_001354975.2:c.625A>G
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NP_001341904.1:p.Asn209Asp
|
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NR_027302.2:n.1030A>G
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NR_149091.2:n.527A>G
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NR_149092.2:n.693A>G
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NR_149093.2:n.1219A>G
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NR_149094.2:n.1113A>G
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