| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267706.1 | 121 | Missense Mutation | CCT,GCT | P5A | NP_001254635.1 |
| NM_001314029.1 | 121 | Missense Mutation | CCT,GCT | P5A | NP_001300958.1 |
| NM_014143.3 | 121 | Missense Mutation | CCT,GCT | P5A | NP_054862.1 |