Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135699.1 | 962 | Intron | NP_001129171.1 | ||
NM_001135700.1 | 962 | Intron | NP_001129172.1 | ||
NM_001135701.1 | 962 | Intron | NP_001129173.1 | ||
NM_001135702.1 | 962 | Intron | NP_001129174.1 | ||
NM_003406.3 | 962 | Intron | NP_003397.1 | ||
NM_145690.2 | 962 | Intron | NP_663723.1 | ||
XM_005251061.3 | 962 | Missense Mutation | AAT,GAT | N143D | XP_005251118.1 |
XM_005251063.3 | 962 | Missense Mutation | AAT,GAT | N143D | XP_005251120.1 |
XM_011517290.2 | 962 | Intron | XP_011515592.1 | ||
XM_017013810.1 | 962 | Missense Mutation | AAT,GAT | N143D | XP_016869299.1 |
XM_017013811.1 | 962 | Missense Mutation | AAT,GAT | N143D | XP_016869300.1 |
XM_017013812.1 | 962 | Intron | XP_016869301.1 |