| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015626.8 | 545 | Missense Mutation | CCA,TCA | P44S | NP_056441.6 |
| NM_134265.2 | 545 | Intron | NP_599027.1 | ||
| XM_005257963.3 | 545 | Intron | XP_005258020.1 | ||
| XM_017024433.1 | 545 | Missense Mutation | CCA,TCA | P44S | XP_016879922.1 |
| XM_017024434.1 | 545 | UTR 5 | XP_016879923.1 | ||
| XM_017024435.1 | 545 | UTR 5 | XP_016879924.1 | ||
| XM_017024436.1 | 545 | Intron | XP_016879925.1 |