| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_198944.1 | 1364 | Intron | NP_945182.1 | ||
| XM_005259853.3 | 1364 | Missense Mutation | CCC,CTC | P287L | XP_005259910.1 |
| XM_011527915.2 | 1364 | Missense Mutation | CCC,CTC | P337L | XP_011526217.1 |