| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000842.4 | 3995 | Missense Mutation | CCT,CTT | P1168L | NP_000833.1 |
| NM_001143831.2 | 3995 | Missense Mutation | CCT,CTT | P1200L | NP_001137303.1 |
| XM_006718828.3 | 3995 | Missense Mutation | CCT,CTT | P1200L | XP_006718891.1 |
| XM_011542792.1 | 3995 | Missense Mutation | CCT,CTT | P1200L | XP_011541094.1 |
| XM_017017627.1 | 3995 | Missense Mutation | CCT,CTT | P1168L | XP_016873116.1 |