| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020823.1 | 79 | Missense Mutation | CCC,TCC | P22S | NP_065874.1 |
| XM_005267074.3 | 79 | Intron | XP_005267131.1 | ||
| XM_011535999.1 | 79 | Missense Mutation | CCC,TCC | P22S | XP_011534301.1 |
| XM_011536000.1 | 79 | Missense Mutation | CCC,TCC | P22S | XP_011534302.1 |
| XM_011536001.2 | 79 | Intron | XP_011534303.1 | ||
| XM_011536002.2 | 79 | Intron | XP_011534304.1 | ||
| XM_011536003.2 | 79 | Missense Mutation | CCC,TCC | P22S | XP_011534305.1 |