| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001284271.1 | 6922 | Intron | NP_001271200.1 | ||
| NM_006828.3 | 6922 | Missense Mutation | CCT,TCT | P2105S | NP_006819.2 |
| NM_022091.4 | 6922 | Intron | NP_071374.1 | ||
| XM_011535394.2 | 6922 | Missense Mutation | CCT,TCT | P2110S | XP_011533696.1 |
| XM_011535395.2 | 6922 | Missense Mutation | CCT,TCT | P2007S | XP_011533697.1 |
| XM_011535396.2 | 6922 | Missense Mutation | CCT,TCT | P2007S | XP_011533698.1 |
| XM_017010205.1 | 6922 | Missense Mutation | CCT,TCT | P2007S | XP_016865694.1 |
| XM_017010206.1 | 6922 | Missense Mutation | CCT,TCT | P1632S | XP_016865695.1 |