| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184722.1 | 448 | Intron | NP_001171651.1 | ||
| NM_001289789.1 | 448 | Intron | NP_001276718.1 | ||
| XM_005258764.2 | 448 | Intron | XP_005258821.1 | ||
| XM_006723148.2 | 448 | Intron | XP_006723211.1 | ||
| XM_011526754.2 | 448 | Missense Mutation | ACC,CCC | T15P | XP_011525056.1 |