| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146726.1 | 1093 | Missense Mutation | AGC,GGC | S346G | NP_001140198.1 |
| NM_138379.2 | 1093 | Missense Mutation | AGC,GGC | S374G | NP_612388.2 |
| XM_011534694.2 | 1093 | Intron | XP_011532996.1 | ||
| XM_017010021.1 | 1093 | Missense Mutation | AGC,GGC | S319G | XP_016865510.1 |