Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000860.5 | 697 | Missense Mutation | AGT,CGT | S174R | NP_000851.2 |
NM_001145816.2 | 697 | Intron | NP_001139288.1 | ||
NM_001256301.1 | 697 | Missense Mutation | AGT,CGT | S53R | NP_001243230.1 |
NM_001256305.1 | 697 | Intron | NP_001243234.1 | ||
NM_001256306.1 | 697 | Missense Mutation | AGT,CGT | S106R | NP_001243235.1 |
NM_001256307.1 | 697 | Missense Mutation | AGT,CGT | S53R | NP_001243236.1 |
XM_011531907.1 | 697 | Intron | XP_011530209.1 |