| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000174.4 | 642 | Missense Mutation | CCT,CTT | P56L | NP_000165.1 |
| XM_005247374.3 | 642 | Missense Mutation | CCT,CTT | P56L | XP_005247431.1 |
| XM_011512701.1 | 642 | Missense Mutation | CCT,CTT | P56L | XP_011511003.1 |
| XM_011512702.1 | 642 | Missense Mutation | CCT,CTT | P56L | XP_011511004.1 |