| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291446.1 | 3245 | Intron | NP_001278375.1 | ||
| NM_001291447.1 | 3245 | Intron | NP_001278376.1 | ||
| NM_005407.2 | 3245 | Missense Mutation | CCT,TCT | P984S | NP_005398.2 |
| XM_011537064.1 | 3245 | Intron | XP_011535366.1 | ||
| XM_011537065.1 | 3245 | Intron | XP_011535367.1 |