| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317958.1 | 1355 | Silent Mutation | CCC,CCG | P269P | NP_001304887.1 |
| NM_001317959.1 | 1355 | Silent Mutation | CCC,CCG | P301P | NP_001304888.1 |
| NM_152572.2 | 1355 | Silent Mutation | CCC,CCG | P473P | NP_689785.1 |
| XM_005272169.2 | 1355 | Silent Mutation | CCC,CCG | P485P | XP_005272226.1 |
| XM_006716965.2 | 1355 | Silent Mutation | CCC,CCG | P401P | XP_006717028.1 |
| XM_011518277.2 | 1355 | Intron | XP_011516579.1 | ||
| XM_011518278.2 | 1355 | Silent Mutation | CCC,CCG | P399P | XP_011516580.1 |
| XM_017014308.1 | 1355 | Silent Mutation | CCC,CCG | P301P | XP_016869797.1 |