Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024746.3 | 2003 | Missense Mutation | TCC,TTC | S648F | NP_079022.2 |
XM_011509985.2 | 2003 | Missense Mutation | TCC,TTC | S667F | XP_011508287.1 |
XM_011509986.1 | 2003 | Intron | XP_011508288.1 | ||
XM_017002350.1 | 2003 | Intron | XP_016857839.1 |