Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001174118.1 | 787 | Missense Mutation | GCC,TCC | A263S | NP_001167589.1 |
NM_203304.3 | 787 | Missense Mutation | GCC,TCC | A263S | NP_976049.3 |
XM_017026811.1 | 787 | Missense Mutation | GCC,TCC | A29S | XP_016882300.1 |