Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018014.3 | 2696 | Silent Mutation | AAA,AAG | K772K | NP_060484.2 |
NM_022893.3 | 2696 | Intron | NP_075044.2 | ||
NM_138559.1 | 2696 | Missense Mutation | AAT,AGT | N239S | NP_612569.1 |
XM_011532909.1 | 2696 | UTR 3 | XP_011531211.1 | ||
XM_011532910.1 | 2696 | Missense Mutation | AAT,AGT | N823S | XP_011531212.1 |
XM_011532912.1 | 2696 | Missense Mutation | AAT,AGT | N789S | XP_011531214.1 |
XM_017004333.1 | 2696 | Intron | XP_016859822.1 | ||
XM_017004334.1 | 2696 | Intron | XP_016859823.1 | ||
XM_017004335.1 | 2696 | Intron | XP_016859824.1 | ||
XM_017004336.1 | 2696 | Intron | XP_016859825.1 | ||
XM_017004337.1 | 2696 | Intron | XP_016859826.1 | ||
XM_017004338.1 | 2696 | Intron | XP_016859827.1 |