Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001168325.1 | 688 | Missense Mutation | CCT,CTT | P148L | NP_001161797.1 |
NM_017899.3 | 688 | Missense Mutation | CCT,CTT | P175L | NP_060369.3 |
XM_011538503.1 | 688 | Missense Mutation | CCT,CTT | P163L | XP_011536805.1 |
XM_017019532.1 | 688 | Intron | XP_016875021.1 | ||
XM_017019533.1 | 688 | Intron | XP_016875022.1 |