Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001024847.2 | 219 | Intron | NP_001020018.1 | ||
NM_003242.5 | 219 | Intron | NP_003233.4 | ||
XM_011534043.2 | 219 | Missense Mutation | AGT,GGT | S6G | XP_011532345.1 |
XM_011534045.2 | 219 | Intron | XP_011532347.1 | ||
XM_017007106.1 | 219 | Intron | XP_016862595.1 |