Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164586.1 | 207 | Missense Mutation | CCT,CGT | P11R | NP_001158058.1 |
XM_005245580.3 | 207 | Missense Mutation | CCT,CGT | P11R | XP_005245637.1 |
XM_006711618.3 | 207 | Missense Mutation | CCT,CGT | P11R | XP_006711681.1 |
XM_011510120.2 | 207 | Missense Mutation | CCT,CGT | P11R | XP_011508422.1 |
XM_011510121.2 | 207 | Missense Mutation | CCT,CGT | P11R | XP_011508423.1 |
XM_017002787.1 | 207 | Missense Mutation | CCT,CGT | P11R | XP_016858276.1 |