| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020958.2 | 248 | Missense Mutation | CCG,TCG | P41S | NP_066009.2 |
| NM_058237.1 | 248 | Missense Mutation | CCG,TCG | P41S | NP_478144.1 |
| XM_005267930.2 | 248 | UTR 5 | XP_005267987.1 | ||
| XM_011537038.2 | 248 | UTR 5 | XP_011535340.1 | ||
| XM_011537039.2 | 248 | Intron | XP_011535341.1 | ||
| XM_011537040.2 | 248 | Intron | XP_011535342.1 | ||
| XM_017021528.1 | 248 | Intron | XP_016877017.1 | ||
| XM_017021529.1 | 248 | UTR 5 | XP_016877018.1 | ||
| XM_017021530.1 | 248 | UTR 5 | XP_016877019.1 |