Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142964.1 | 494 | Missense Mutation | CCA,TCA | P137S | NP_001136436.1 |
XM_011530373.2 | 494 | Missense Mutation | CCA,TCA | P137S | XP_011528675.1 |
XM_017028939.1 | 494 | UTR 5 | XP_016884428.1 |