| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001206920.1 | 1518 | Missense Mutation | CCT,TCT | P401S | NP_001193849.1 |
| NM_001306087.1 | 1518 | Missense Mutation | CCT,TCT | P402S | NP_001293016.1 |
| XM_011536720.2 | 1518 | Missense Mutation | CCT,TCT | P449S | XP_011535022.1 |
| XM_011536721.2 | 1518 | Missense Mutation | CCT,TCT | P448S | XP_011535023.1 |
| XM_011536723.2 | 1518 | Missense Mutation | CCT,TCT | P389S | XP_011535025.1 |
| XM_011536724.2 | 1518 | Missense Mutation | CCT,TCT | P384S | XP_011535026.1 |
| XM_011536725.1 | 1518 | Missense Mutation | CCT,TCT | P279S | XP_011535027.1 |
| XM_017021258.1 | 1518 | Missense Mutation | CCT,TCT | P449S | XP_016876747.1 |
| XM_017021259.1 | 1518 | Intron | XP_016876748.1 | ||
| XM_017021260.1 | 1518 | Missense Mutation | CCT,TCT | P279S | XP_016876749.1 |
| XM_017021261.1 | 1518 | Intron | XP_016876750.1 |