Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_207396.2 | 388 | Missense Mutation | CCC,TCC | P72S | NP_997279.2 |
XM_011541439.2 | 388 | Intron | XP_011539741.1 | ||
XM_017001259.1 | 388 | Missense Mutation | CCC,TCC | P72S | XP_016856748.1 |