| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001007125.1 | 461 | Missense Mutation | ACC,CCC | T131P | NP_001007126.1 |
| XM_005260200.3 | 461 | Missense Mutation | ACC,CCC | T131P | XP_005260257.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000913.5 | 461 | Intron | NP_000904.1 | ||
| NM_001200019.1 | 461 | Intron | NP_001186948.1 | ||
| NM_001318853.1 | 461 | Intron | NP_001305782.1 | ||
| NM_001318854.1 | 461 | Intron | NP_001305783.1 | ||
| NM_001318855.1 | 461 | Intron | NP_001305784.1 | ||
| NM_182647.3 | 461 | Intron | NP_872588.1 | ||
| XM_011528828.2 | 461 | Intron | XP_011527130.1 | ||
| XM_011528830.2 | 461 | Intron | XP_011527132.1 | ||
| XM_017027852.1 | 461 | Intron | XP_016883341.1 | ||
| XM_017027853.1 | 461 | Intron | XP_016883342.1 | ||
| XM_017027854.1 | 461 | Intron | XP_016883343.1 | ||
| XM_017027855.1 | 461 | Intron | XP_016883344.1 |