Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171873.1 | 1447 | Intron | NP_001165344.1 | ||
NM_152404.3 | 1447 | Missense Mutation | ATG,GTG | M509V | NP_689617.3 |
XM_005248243.4 | 1447 | Missense Mutation | ATG,GTG | M455V | XP_005248300.1 |
XM_011513957.2 | 1447 | Missense Mutation | ATG,GTG | M478V | XP_011512259.1 |
XM_011513958.2 | 1447 | Missense Mutation | ATG,GTG | M475V | XP_011512260.1 |
XM_011513959.2 | 1447 | Missense Mutation | ATG,GTG | M455V | XP_011512261.1 |
XM_011513961.2 | 1447 | Missense Mutation | ATG,GTG | M396V | XP_011512263.1 |