| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_080675.3 | 880 | Missense Mutation | ATC,CTC | I263L | NP_542406.2 |
| XM_011528573.1 | 880 | Missense Mutation | ATC,CTC | I286L | XP_011526875.1 |
| XM_011528574.1 | 880 | Missense Mutation | ATC,CTC | I238L | XP_011526876.1 |
| XM_011528575.1 | 880 | Missense Mutation | ATC,CTC | I173L | XP_011526877.1 |
| XM_011528576.1 | 880 | Intron | XP_011526878.1 |