| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017742.5 | 19 | Missense Mutation | ACG,ATG | T81M | NP_060212.4 |
| XM_006722493.3 | 19 | Missense Mutation | ACG,ATG | T1M | XP_006722556.1 |
| XM_011526044.1 | 19 | Intron | XP_011524346.1 | ||
| XM_017025802.1 | 19 | Missense Mutation | ACG,ATG | T1M | XP_016881291.1 |