| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001161452.1 | 1488 | Missense Mutation | GGG,GTG | G214V | NP_001154924.1 |
| NM_001161454.1 | 1488 | Missense Mutation | GGG,GTG | G231V | NP_001154926.1 |
| NM_001300763.1 | 1488 | Missense Mutation | GGG,GTG | G214V | NP_001287692.1 |
| NM_153611.4 | 1488 | Missense Mutation | GGG,GTG | G214V | NP_705839.3 |
| XM_011544821.1 | 1488 | Missense Mutation | GGG,GTG | G231V | XP_011543123.1 |
| XM_011544823.1 | 1488 | Missense Mutation | GGG,GTG | G214V | XP_011543125.1 |
| XM_011544824.1 | 1488 | Intron | XP_011543126.1 | ||
| XM_017017345.1 | 1488 | Missense Mutation | GGG,GTG | G231V | XP_016872834.1 |
| XM_017017346.1 | 1488 | Missense Mutation | GGG,GTG | G214V | XP_016872835.1 |
| XM_017017347.1 | 1488 | Missense Mutation | GGG,GTG | G95V | XP_016872836.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015533.3 | 1488 | Intron | NP_056348.2 | ||
| XM_011544912.2 | 1488 | Intron | XP_011543214.1 | ||
| XM_017017517.1 | 1488 | Intron | XP_016873006.1 | ||
| XM_017017518.1 | 1488 | Intron | XP_016873007.1 | ||
| XM_017017519.1 | 1488 | Intron | XP_016873008.1 | ||
| XM_017017520.1 | 1488 | Intron | XP_016873009.1 | ||
| XM_017017521.1 | 1488 | Intron | XP_016873010.1 | ||
| XM_017017522.1 | 1488 | Intron | XP_016873011.1 | ||
| XM_017017523.1 | 1488 | Intron | XP_016873012.1 | ||
| XM_017017524.1 | 1488 | Intron | XP_016873013.1 |