Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002136.3 | 655 | Intron | NP_002127.1 | ||
NM_031157.3 | 655 | Intron | NP_112420.1 | ||
XM_005268826.1 | 655 | Silent Mutation | CTC,CTG | L181L | XP_005268883.1 |
XM_017019251.1 | 655 | Intron | XP_016874740.1 |