Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001287147.1 | 1160 | Intron | NP_001274076.1 | ||
NM_178176.3 | 1160 | Intron | NP_835470.1 | ||
XM_005250309.3 | 1160 | Missense Mutation | CCT,TCT | P295S | XP_005250366.1 |
XM_011516126.2 | 1160 | Intron | XP_011514428.1 | ||
XM_011516127.2 | 1160 | Intron | XP_011514429.1 |