| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184965.1 | 472 | Missense Mutation | CCT,CGT | P14R | NP_001171894.1 |
| NM_001184966.1 | 472 | Missense Mutation | CCT,CGT | P14R | NP_001171895.1 |
| NM_019045.4 | 472 | Missense Mutation | CCT,CGT | P14R | NP_061918.3 |
| XM_011531353.2 | 472 | Missense Mutation | CCT,CGT | P14R | XP_011529655.1 |
| XM_017029600.1 | 472 | UTR 5 | XP_016885089.1 |