Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005898.4 | 313 | Missense Mutation | CCC,TCC | P42S | NP_005889.3 |
NM_203364.2 | 313 | Missense Mutation | CCC,TCC | P42S | NP_976240.1 |
XM_017017749.1 | 313 | Missense Mutation | CCC,TCC | P42S | XP_016873238.1 |