Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005371.5 | 699 | Missense Mutation | CCC,CTC | P178L | NP_005362.3 |
NM_023033.3 | 699 | Silent Mutation | TCC,TCT | S116S | NP_075422.3 |
XM_005268873.2 | 699 | Missense Mutation | CCC,CTC | P135L | XP_005268930.1 |
XM_017019305.1 | 699 | Missense Mutation | CCC,CTC | P203L | XP_016874794.1 |