Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016262.4 | 1447 | Missense Mutation | TCC,TTC | S440F | NP_057346.1 |
XM_011535875.2 | 1447 | Missense Mutation | TCC,TTC | S365F | XP_011534177.1 |
XM_017010918.1 | 1447 | Missense Mutation | TCC,TTC | S396F | XP_016866407.1 |