Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_198489.2 | 102 | Missense Mutation | ACC,GCC | T13A | NP_940891.1 |
XM_011542799.1 | 102 | Intron | XP_011541101.1 | ||
XM_011542800.2 | 102 | Intron | XP_011541102.1 | ||
XM_017017652.1 | 102 | UTR 5 | XP_016873141.1 |