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Items: 6

1.

transmembrane protein 106A isoform X3 [Homo sapiens]

214 aa protein

  • Record suppressed.This record was removed as a result of standard genome annotation processing. Please see www.ncbi.nlm.nih.gov/genome/annotation_euk/process/ for more information.
Accession:
XP_016879603.1
GI:
1034597985

GenPept Identical Proteins FASTA Graphics 
2.

transmembrane protein 106A isoform a [Homo sapiens]

262 aa protein

Accession:
NP_001278515.1
GI:
615276263

BioProject Nucleotide PubMed Taxonomy

GenPept Identical Proteins FASTA Graphics 
3.

transmembrane protein 106A isoform b [Homo sapiens]

214 aa protein

Accession:
NP_001278516.1
GI:
615276252

BioProject Nucleotide PubMed Taxonomy

GenPept Identical Proteins FASTA Graphics 
4.

transmembrane protein 106A isoform X3 [Homo sapiens]

214 aa protein

  • Record suppressed.This record was removed as a result of standard genome annotation processing. Please see www.ncbi.nlm.nih.gov/genome/annotation_euk/process/ for more information.
Accession:
XP_006721722.1
GI:
578830320

GenPept Identical Proteins FASTA Graphics 
5.

transmembrane protein 106A isoform X1 [Homo sapiens]

262 aa protein

  • Record suppressed.This record was removed as a result of standard genome annotation processing. Please see www.ncbi.nlm.nih.gov/genome/annotation_euk/process/ for more information.
Accession:
XP_006721721.1
GI:
578830316

GenPept Identical Proteins FASTA Graphics 
6.

transmembrane protein 106A isoform a [Homo sapiens]

262 aa protein

Accession:
NP_659478.1
GI:
21450796

BioProject Nucleotide PubMed Taxonomy

GenPept Identical Proteins FASTA Graphics 
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Analyze these sequences

  • Run BLAST
    Find regions of similarity between these sequences and other sequences using BLAST.
  • Align sequences with COBALT
    Align multiple protein sequences with COBALT, which computes an alignment using conserved domain and local sequence similarity information.
  • Identify Conserved Domains with CD-Search
    Use Conserved Domain Search (CD-search) to identify conserved domains in these protein sequences compared against conserved domain models.

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