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neuropilin-1 isoform c precursor [Homo sapiens]

NCBI Reference Sequence: NP_001019800.2

Identical Proteins FASTA Graphics 

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  • neuropilin-1 isoform c precursor [Homo sapiens]
    neuropilin-1 isoform c precursor [Homo sapiens]
    gi|1844084081|ref|NP_001019800.2|
    Protein
  • Werner Syndrome
    Werner Syndrome
    An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a t...<br/>Year introduced: 1998
    MeSH

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