| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001102612.2 | 765 | Missense Mutation | CCG,CTG | P155L | NP_001096082.2 |
| NM_001167902.1 | 765 | Intron | NP_001161374.1 | ||
| XM_011521254.1 | 765 | Missense Mutation | CCG,CTG | P246L | XP_011519556.1 |
| XM_017021933.1 | 765 | Missense Mutation | CCG,CTG | P101L | XP_016877422.1 |