| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001139517.1 | 907 | Missense Mutation | CCT,CTT | P211L | NP_001132989.1 |
| NM_001139518.1 | 907 | Missense Mutation | CCT,CTT | P197L | NP_001132990.1 |
| NM_001316362.1 | 907 | Missense Mutation | CCT,CTT | P109L | NP_001303291.1 |
| NM_003690.4 | 907 | Missense Mutation | CCT,CTT | P222L | NP_003681.1 |
| XM_011512063.1 | 907 | Missense Mutation | CCT,CTT | P137L | XP_011510365.1 |
| XM_011512066.1 | 907 | Missense Mutation | CCT,CTT | P109L | XP_011510368.1 |
| XM_017005159.1 | 907 | Missense Mutation | CCT,CTT | P109L | XP_016860648.1 |