| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130167.1 | 600 | Missense Mutation | ACC,TCC | T168S | NP_001123639.1 |
| NM_001130168.1 | 600 | Missense Mutation | ACC,TCC | T46S | NP_001123640.1 |
| NM_182707.2 | 600 | Missense Mutation | ACC,TCC | T168S | NP_874366.1 |
| XM_011526986.1 | 600 | Intron | XP_011525288.1 | ||
| XM_011526987.2 | 600 | Intron | XP_011525289.1 | ||
| XM_011526988.2 | 600 | Intron | XP_011525290.1 |