serpin B6 isoform X1 [Homo sapiens]

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Copy number variants are a common cause of non-syndromic hearing loss. [Genome Med. 2014]
Copy number variants are a common cause of non-syndromic hearing loss.
Shearer AE, Kolbe DL, Azaiez H, Sloan CM, Frees KL, Weaver AE, Clark ET, Nishimura CJ, Black-Ziegelbein EA, Smith RJ. Genome Med. 2014; 6(5):37. Epub 2014 May 22.
Human cytoplasmic antiproteinase neutralizes rapidly and efficiently chymotrypsin and trypsin-like proteases utilizing distinct reactive site residues. [J Biol Chem. 1996]
Human cytoplasmic antiproteinase neutralizes rapidly and efficiently chymotrypsin and trypsin-like proteases utilizing distinct reactive site residues.
Riewald M, Schleef RR. J Biol Chem. 1996 Jun 14; 271(24):14526-32.
Identification and characterization of the cytoplasmic antiproteinase (CAP) in human platelets. Evidence for the interaction of CAP with endogenous platelet proteins. [J Biol Chem. 1996]
Identification and characterization of the cytoplasmic antiproteinase (CAP) in human platelets. Evidence for the interaction of CAP with endogenous platelet proteins.
Riewald M, Morgenstern KA, Schleef RR. J Biol Chem. 1996 Mar 22; 271(12):7160-7.

RefSeq genomic sequence
See the genomic reference sequence for the SERPINB6 gene (NG_027692.1).
RefSeq mRNA
See reference mRNA sequence for the SERPINB6 gene (XM_054355632.1).

serpin B6 isoform X1 [Homo sapiens]
serpin B6 isoform X1 [Homo sapiens]
gi|2462608889|ref|XP_054211607.1|

Protein
PREDICTED: Homo sapiens serpin family B member 6 (SERPINB6), transcript variant ...
PREDICTED: Homo sapiens serpin family B member 6 (SERPINB6), transcript variant X4, mRNA
gi|2462608890|ref|XM_054355633.1|

Nucleotide

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Protein