Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001122870.2 | 663 | Missense Mutation | CCA,TCA | P36S | NP_001116342.1 |
NM_144641.3 | 663 | Missense Mutation | CCA,TCA | P248S | NP_653242.3 |
XM_005264879.2 | 663 | Missense Mutation | CCA,TCA | P248S | XP_005264936.1 |
XM_005264880.3 | 663 | Missense Mutation | CCA,TCA | P163S | XP_005264937.1 |
XM_005264881.1 | 663 | Missense Mutation | CCA,TCA | P87S | XP_005264938.1 |