| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006821.5 | 803 | Intron | NP_006812.3 | ||
| XM_006720007.1 | 803 | Missense Mutation | CCT,CTT | P19L | XP_006720070.1 |
| XM_017020937.1 | 803 | Missense Mutation | CCT,CTT | P216L | XP_016876426.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001220484.1 | 803 | Intron | NP_001207413.1 | ||
| NM_203309.2 | 803 | Intron | NP_976054.2 | ||
| XM_006720143.2 | 803 | Intron | XP_006720206.1 | ||
| XM_011536760.2 | 803 | Intron | XP_011535062.1 | ||
| XM_011536761.2 | 803 | Intron | XP_011535063.1 | ||
| XM_017021289.1 | 803 | Intron | XP_016876778.1 |