| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_175852.3 | 222 | Missense Mutation | AGC,CGC | S48R | NP_787048.1 |
| XM_011540931.2 | 222 | UTR 5 | XP_011539233.1 | ||
| XM_011540932.2 | 222 | Intron | XP_011539234.1 | ||
| XM_017000561.1 | 222 | Missense Mutation | AGC,CGC | S48R | XP_016856050.1 |
| XM_017000562.1 | 222 | Missense Mutation | AGC,CGC | S48R | XP_016856051.1 |
| XM_017000563.1 | 222 | Missense Mutation | AGC,CGC | S48R | XP_016856052.1 |
| XM_017000564.1 | 222 | Intron | XP_016856053.1 | ||
| XM_017000565.1 | 222 | Intron | XP_016856054.1 |