| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282688.1 | 332 | Silent Mutation | CCA,CCG | P58P | NP_001269617.1 |
| NM_001282689.1 | 332 | Missense Mutation | AGT,GGT | S26G | NP_001269618.1 |
| NM_001282690.1 | 332 | UTR 5 | NP_001269619.1 | ||
| NM_024077.4 | 332 | Silent Mutation | CCA,CCG | P58P | NP_076982.3 |
| XM_005252196.2 | 332 | Silent Mutation | CCA,CCG | P58P | XP_005252253.1 |
| XM_005252202.3 | 332 | Intron | XP_005252259.1 | ||
| XM_006717282.2 | 332 | Missense Mutation | AGT,GGT | S26G | XP_006717345.1 |
| XM_011519000.2 | 332 | UTR 5 | XP_011517302.1 | ||
| XM_011519001.1 | 332 | UTR 5 | XP_011517303.1 | ||
| XM_011519002.1 | 332 | UTR 5 | XP_011517304.1 | ||
| XM_011519003.1 | 332 | UTR 5 | XP_011517305.1 | ||
| XM_017015122.1 | 332 | Silent Mutation | CCA,CCG | P58P | XP_016870611.1 |
| XM_017015123.1 | 332 | Silent Mutation | CCA,CCG | P58P | XP_016870612.1 |
| XM_017015124.1 | 332 | Silent Mutation | CCA,CCG | P58P | XP_016870613.1 |
| XM_017015125.1 | 332 | Intron | XP_016870614.1 |