Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016246.2 | 2698 | Intron | NP_057330.2 | ||
XM_005258969.3 | 2698 | Intron | XP_005259026.1 | ||
XM_005258970.3 | 2698 | Intron | XP_005259027.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001161354.1 | 2698 | UTR 3 | NP_001154826.1 | ||
NM_020904.2 | 2698 | Missense Mutation | ACG,GCG | T714A | NP_065955.2 |
XM_005259107.2 | 2698 | Missense Mutation | ACG,GCG | T689A | XP_005259164.1 |
XM_006723301.2 | 2698 | UTR 3 | XP_006723364.1 | ||
XM_011527157.1 | 2698 | Missense Mutation | ACG,GCG | T718A | XP_011525459.1 |
XM_011527158.2 | 2698 | Missense Mutation | ACG,GCG | T682A | XP_011525460.1 |
XM_011527159.1 | 2698 | Missense Mutation | ACG,GCG | T678A | XP_011525461.1 |
XM_011527160.1 | 2698 | UTR 3 | XP_011525462.1 | ||
XM_011527162.2 | 2698 | Missense Mutation | ACG,GCG | T369A | XP_011525464.1 |
XM_017027037.1 | 2698 | Missense Mutation | ACG,GCG | T591A | XP_016882526.1 |