| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199138.1 | 3206 | Missense Mutation | CAA,CTA | Q1021L | NP_001186067.1 |
| NM_001199139.1 | 3206 | Missense Mutation | CAA,CTA | Q1021L | NP_001186068.1 |
| NM_001302504.1 | 3206 | Missense Mutation | CAA,CTA | Q356L | NP_001289433.1 |
| NM_021209.4 | 3206 | Missense Mutation | CAA,CTA | Q1021L | NP_067032.3 |
| XM_017004619.1 | 3206 | Intron | XP_016860108.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| XM_006712048.3 | 3206 | UTR 3 | XP_006712111.1 | ||
| XM_011532959.2 | 3206 | UTR 3 | XP_011531261.1 | ||
| XM_011532960.2 | 3206 | UTR 3 | XP_011531262.1 | ||
| XM_011532961.2 | 3206 | UTR 3 | XP_011531263.1 | ||
| XM_011532962.2 | 3206 | UTR 3 | XP_011531264.1 | ||
| XM_011532963.2 | 3206 | Intron | XP_011531265.1 | ||
| XM_017004462.1 | 3206 | UTR 3 | XP_016859951.1 | ||
| XM_017004463.1 | 3206 | Intron | XP_016859952.1 | ||
| XM_017004464.1 | 3206 | Intron | XP_016859953.1 | ||
| XM_017004465.1 | 3206 | Intron | XP_016859954.1 | ||
| XM_017004466.1 | 3206 | Intron | XP_016859955.1 |