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- accession：NM_001272037
- 基因别名：TSPEAR
- 基因描述：Homo sapiens thrombospondin-type laminin G domain and EAR repeats (TSPEAR), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：1806
- 翻译后氨基酸长度：601
- TranscriptVariant：This variant (2) contains an additional exon in the 5' region that causes translation initiation from a downstream AUG compared to variant 1. The resulting isoform (2) has a shorter N-terminus compared to isoform 1.
- 基因简介：This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
- 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
