| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_053002.5 | 1330 | Intron | NP_443728.3 | ||
| XM_006713487.3 | 1330 | Intron | XP_006713550.1 | ||
| XM_011512390.2 | 1330 | Intron | XP_011510692.1 | ||
| XM_011512394.2 | 1330 | Intron | XP_011510696.1 | ||
| XM_011512399.2 | 1330 | Intron | XP_011510701.1 | ||
| XM_017005676.1 | 1330 | Intron | XP_016861165.1 | ||
| XM_017005677.1 | 1330 | Intron | XP_016861166.1 | ||
| XM_017005678.1 | 1330 | Intron | XP_016861167.1 | ||
| XM_017005679.1 | 1330 | Intron | XP_016861168.1 | ||
| XM_017005680.1 | 1330 | Intron | XP_016861169.1 | ||
| XM_017005681.1 | 1330 | Intron | XP_016861170.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022788.4 | 1330 | Missense Mutation | ACT,CCT | T258P | NP_073625.1 |
| NM_176876.2 | 1330 | Missense Mutation | ACT,CCT | T258P | NP_795345.1 |
| XM_017007069.1 | 1330 | Missense Mutation | ACT,CCT | T258P | XP_016862558.1 |