| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001104587.1 | 2628 | Intron | NP_001098057.1 | ||
| NM_001104588.1 | 2628 | Intron | NP_001098058.1 | ||
| NM_001104589.1 | 2628 | Intron | NP_001098059.1 | ||
| NM_001104590.1 | 2628 | Intron | NP_001098060.1 | ||
| NM_152270.3 | 2628 | Intron | NP_689483.3 | ||
| XM_005258068.3 | 2628 | Missense Mutation | CCT,TCT | P765S | XP_005258125.1 |
| XM_006722171.3 | 2628 | Missense Mutation | CCT,TCT | P765S | XP_006722234.1 |
| XM_011525465.2 | 2628 | Missense Mutation | CCT,TCT | P765S | XP_011523767.1 |
| XM_017025299.1 | 2628 | Missense Mutation | CCT,TCT | P765S | XP_016880788.1 |