Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001560.2 | 405 | Intron | NP_001551.1 | ||
XM_011531336.1 | 405 | Missense Mutation | TTG,TTT | L130F | XP_011529638.1 |
XM_011531337.1 | 405 | Intron | XP_011529639.1 | ||
XM_017029507.1 | 405 | Intron | XP_016884996.1 |