Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018163.2 | 536 | Intron | NP_060633.1 | ||
XM_017022401.1 | 536 | Intron | XP_016877890.1 | ||
XM_017022402.1 | 536 | Intron | XP_016877891.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077268.1 | 536 | Missense Mutation | CCC,TCC | P8S | NP_001070736.1 |
NM_001258420.1 | 536 | Missense Mutation | CCC,TCC | P8S | NP_001245349.1 |
NM_001258421.1 | 536 | UTR 5 | NP_001245350.1 | ||
NM_032850.4 | 536 | Intron | NP_116239.3 | ||
XM_017022683.1 | 536 | Intron | XP_016878172.1 | ||
XM_017022684.1 | 536 | Missense Mutation | CCC,TCC | P8S | XP_016878173.1 |