| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001316973.1 | 857 | Missense Mutation | CTT,TTT | L171F | NP_001303902.1 |
| NM_001316974.1 | 857 | Missense Mutation | CTT,TTT | L192F | NP_001303903.1 |
| NM_001316975.1 | 857 | Missense Mutation | CTT,TTT | L171F | NP_001303904.1 |
| NM_001316976.1 | 857 | Intron | NP_001303905.1 | ||
| NM_032368.4 | 857 | Missense Mutation | CTT,TTT | L171F | NP_115744.2 |
| XM_005263506.2 | 857 | Missense Mutation | CTT,TTT | L171F | XP_005263563.1 |
| XM_005263509.2 | 857 | Intron | XP_005263566.1 | ||
| XM_017002546.1 | 857 | Missense Mutation | CTT,TTT | L171F | XP_016858035.1 |
| XM_017002547.1 | 857 | Missense Mutation | CTT,TTT | L171F | XP_016858036.1 |