| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039885.2 | 268 | Missense Mutation | CGT,CTT | R41L | NP_001034974.1 |
| NM_024301.4 | 268 | Missense Mutation | CGT,CTT | R41L | NP_077277.1 |
| XM_005259247.2 | 268 | Missense Mutation | CGT,CTT | R41L | XP_005259304.1 |
| XM_005259248.2 | 268 | Missense Mutation | CGT,CTT | R41L | XP_005259305.1 |
| XM_005259249.4 | 268 | Missense Mutation | CGT,CTT | R41L | XP_005259306.1 |
| XM_011527306.1 | 268 | Missense Mutation | CGT,CTT | R41L | XP_011525608.1 |
| XM_011527307.1 | 268 | Missense Mutation | CGT,CTT | R41L | XP_011525609.1 |
| XM_017027297.1 | 268 | Missense Mutation | CGT,CTT | R41L | XP_016882786.1 |