| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006500.2 | 1752 | Missense Mutation | ACC,AGC | T606S | NP_006491.2 |
| XM_017017759.1 | 1752 | Missense Mutation | ACC,AGC | T585S | XP_016873248.1 |
| XM_017017760.1 | 1752 | Missense Mutation | ACC,AGC | T574S | XP_016873249.1 |
| XM_017017761.1 | 1752 | Intron | XP_016873250.1 | ||
| XM_017017762.1 | 1752 | Intron | XP_016873251.1 |