Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014299.2 | 3964 | Intron | NP_055114.1 | ||
NM_058243.2 | 3964 | Missense Mutation | ACT,GCT | T1248A | NP_490597.1 |
XM_011527854.1 | 3964 | Missense Mutation | ACT,GCT | T1248A | XP_011526156.1 |
XM_011527855.1 | 3964 | Intron | XP_011526157.1 | ||
XM_011527856.2 | 3964 | Intron | XP_011526158.1 |