| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001083961.1 | 332 | Missense Mutation | AGC,GGC | S81G | NP_001077430.1 |
| NM_173636.4 | 332 | Missense Mutation | AGC,GGC | S81G | NP_775907.4 |
| XM_005258809.2 | 332 | Missense Mutation | AGC,GGC | S81G | XP_005258866.1 |
| XM_011526837.1 | 332 | Missense Mutation | AGC,GGC | S81G | XP_011525139.1 |
| XM_011526838.1 | 332 | Missense Mutation | AGC,GGC | S81G | XP_011525140.1 |
| XM_011526839.1 | 332 | Missense Mutation | AGC,GGC | S81G | XP_011525141.1 |
| XM_011526840.2 | 332 | Intron | XP_011525142.1 | ||
| XM_011526841.2 | 332 | Intron | XP_011525143.1 | ||
| XM_011526842.1 | 332 | Intron | XP_011525144.1 | ||
| XM_011526843.1 | 332 | Intron | XP_011525145.1 | ||
| XM_011526844.2 | 332 | Intron | XP_011525146.1 | ||
| XM_017026665.1 | 332 | Missense Mutation | AGC,GGC | S81G | XP_016882154.1 |