| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001013848.3 | 227 | Missense Mutation | ACC,AGC | T9S | NP_001013870.1 |
| NM_001319194.1 | 227 | Missense Mutation | ACC,AGC | T30S | NP_001306123.1 |
| NM_001319195.1 | 227 | Intron | NP_001306124.1 | ||
| NM_001319200.1 | 227 | Intron | NP_001306129.1 | ||
| NM_019053.5 | 227 | Intron | NP_061926.3 | ||
| XM_017016344.1 | 227 | Missense Mutation | ACC,AGC | T30S | XP_016871833.1 |
| XM_017016345.1 | 227 | Missense Mutation | ACC,AGC | T9S | XP_016871834.1 |
| XM_017016346.1 | 227 | Missense Mutation | ACC,AGC | T9S | XP_016871835.1 |
| XM_017016347.1 | 227 | Intron | XP_016871836.1 | ||
| XM_017016348.1 | 227 | Missense Mutation | ACC,AGC | T30S | XP_016871837.1 |