Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080404.2 | 1127 | Missense Mutation | ATT,GTT | I321V | NP_001073873.2 |
XM_017027195.1 | 1127 | Intron | XP_016882684.1 | ||
XM_017027196.1 | 1127 | Intron | XP_016882685.1 |