| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001085401.2 | 895 | Intron | NP_001078870.1 | ||
| XM_005249112.3 | 895 | Intron | XP_005249169.1 | ||
| XM_011514613.2 | 895 | Intron | XP_011512915.1 | ||
| XM_017010861.1 | 895 | Intron | XP_016866350.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166010.1 | 895 | Missense Mutation | CCT,TCT | P292S | NP_001159482.1 |
| NM_006117.2 | 895 | Missense Mutation | CCT,TCT | P292S | NP_006108.2 |
| NM_206836.2 | 895 | Missense Mutation | CCT,TCT | P322S | NP_996667.2 |
| XM_006714957.1 | 895 | Missense Mutation | CCT,TCT | P292S | XP_006715020.1 |
| XM_017010170.1 | 895 | Missense Mutation | CCT,TCT | P262S | XP_016865659.1 |