Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015470.2 | 4002 | Missense Mutation | AAT,GAT | N603D | NP_056285.1 |
XM_005264251.3 | 4002 | Missense Mutation | AAT,GAT | N1168D | XP_005264308.1 |
XM_005264252.3 | 4002 | Missense Mutation | AAT,GAT | N1274D | XP_005264309.1 |
XM_005264253.4 | 4002 | Intron | XP_005264310.1 | ||
XM_006711985.3 | 4002 | Missense Mutation | AAT,GAT | N1199D | XP_006712048.1 |
XM_011532753.2 | 4002 | Missense Mutation | AAT,GAT | N1068D | XP_011531055.1 |
XM_011532754.2 | 4002 | Intron | XP_011531056.1 | ||
XM_011532755.2 | 4002 | Intron | XP_011531057.1 | ||
XM_011532756.2 | 4002 | Intron | XP_011531058.1 | ||
XM_017003788.1 | 4002 | Missense Mutation | AAT,GAT | N1023D | XP_016859277.1 |