| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| XM_006712048.3 | 266 | Intron | XP_006712111.1 | ||
| XM_011532959.2 | 266 | Missense Mutation | CTT,TTT | L72F | XP_011531261.1 |
| XM_011532960.2 | 266 | Missense Mutation | CTT,TTT | L23F | XP_011531262.1 |
| XM_011532961.2 | 266 | Intron | XP_011531263.1 | ||
| XM_011532962.2 | 266 | Intron | XP_011531264.1 | ||
| XM_011532963.2 | 266 | Missense Mutation | CTT,TTT | L72F | XP_011531265.1 |
| XM_017004462.1 | 266 | Intron | XP_016859951.1 | ||
| XM_017004463.1 | 266 | Missense Mutation | CTT,TTT | L72F | XP_016859952.1 |
| XM_017004464.1 | 266 | Missense Mutation | CTT,TTT | L72F | XP_016859953.1 |
| XM_017004465.1 | 266 | Missense Mutation | CTT,TTT | L72F | XP_016859954.1 |
| XM_017004466.1 | 266 | Missense Mutation | CTT,TTT | L72F | XP_016859955.1 |