| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243313.1 | 239 | Missense Mutation | CCT,TCT | P98S | NP_001230242.1 |
| NM_015690.4 | 239 | Missense Mutation | CCT,TCT | P98S | NP_056505.2 |
| XM_005246464.1 | 239 | Missense Mutation | CCT,TCT | P98S | XP_005246521.1 |
| XM_011510959.1 | 239 | Missense Mutation | CCT,TCT | P98S | XP_011509261.1 |
| XM_011510960.1 | 239 | Missense Mutation | CCT,TCT | P44S | XP_011509262.1 |
| XM_011510961.1 | 239 | Intron | XP_011509263.1 | ||
| XM_017003804.1 | 239 | Missense Mutation | CCT,TCT | P98S | XP_016859293.1 |
| XM_017003805.1 | 239 | UTR 5 | XP_016859294.1 |