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- accession：NM_001003841
- 基因别名：SLC6A19
- 基因描述：Homo sapiens solute carrier family 6 (neutral amino acid transporter), member 19 (SLC6A19), mRNA.
- 载体：现货载体
- CDS区长度：1905
- 翻译后氨基酸长度：634
- 基因简介：This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
