| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199196.1 | 554 | Missense Mutation | CCT,CTT | P77L | NP_001186125.1 |
| NM_033415.3 | 554 | Missense Mutation | CCT,CTT | P52L | NP_219483.1 |
| XM_005260157.3 | 554 | Missense Mutation | CCT,CTT | P52L | XP_005260214.1 |
| XM_017027484.1 | 554 | Missense Mutation | CCT,CTT | P52L | XP_016882973.1 |
| XM_017027485.1 | 554 | Missense Mutation | CCT,CTT | P52L | XP_016882974.1 |