| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_181744.3 | 82 | Missense Mutation | CTT,TTT | L18F | NP_859528.1 |
| XM_017010409.1 | 82 | Intron | XP_016865898.1 | ||
| XM_017010410.1 | 82 | Intron | XP_016865899.1 | ||
| XM_017010411.1 | 82 | Intron | XP_016865900.1 | ||
| XM_017010412.1 | 82 | Intron | XP_016865901.1 | ||
| XM_017010413.1 | 82 | Intron | XP_016865902.1 | ||
| XM_017010414.1 | 82 | Intron | XP_016865903.1 | ||
| XM_017010415.1 | 82 | Intron | XP_016865904.1 | ||
| XM_017010416.1 | 82 | Missense Mutation | CTT,TTT | L18F | XP_016865905.1 |