| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_207111.3 | 2755 | Silent Mutation | CCA,CCG | P919P | NP_996994.1 |
| NM_207116.2 | 2755 | Silent Mutation | CCA,CCG | P862P | NP_996999.1 |
| XM_005249785.2 | 2755 | Silent Mutation | CCA,CCG | P919P | XP_005249842.1 |
| XM_011515436.1 | 2755 | Silent Mutation | CCA,CCG | P484P | XP_011513738.1 |
| XM_017012363.1 | 2755 | Silent Mutation | CCA,CCG | P862P | XP_016867852.1 |
| XM_017012364.1 | 2755 | Intron | XP_016867853.1 | ||
| XM_017012365.1 | 2755 | Silent Mutation | CCA,CCG | P484P | XP_016867854.1 |