| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317911.1 | 853 | Intron | NP_001304840.1 | ||
| NM_001317912.1 | 853 | Intron | NP_001304841.1 | ||
| NM_139245.3 | 853 | Missense Mutation | CTT,GTT | L26V | NP_640338.2 |
| XM_011512440.2 | 853 | Missense Mutation | CTT,GTT | L26V | XP_011510742.1 |