Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001018088.2 | 11055 | Intron | NP_001018098.1 | ||
NM_017684.4 | 11055 | Missense Mutation | TCT,TGT | S3612C | NP_060154.3 |
NM_018080.3 | 11055 | Intron | NP_060550.2 | ||
NM_020821.2 | 11055 | Missense Mutation | TCT,TGT | S3655C | NP_065872.1 |
XM_011521713.2 | 11055 | Intron | XP_011520015.1 | ||
XM_011521714.2 | 11055 | Intron | XP_011520016.1 |