Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022773.2 | 2258 | Missense Mutation | CGT,TGT | R559C | NP_073610.2 |
XM_006720928.2 | 2258 | Missense Mutation | CGT,TGT | R450C | XP_006720991.1 |
XM_006720929.3 | 2258 | Missense Mutation | CGT,TGT | R426C | XP_006720992.1 |
XM_011522614.2 | 2258 | Intron | XP_011520916.1 | ||
XM_011522615.1 | 2258 | Intron | XP_011520917.1 | ||
XM_011522617.2 | 2258 | Missense Mutation | CGT,TGT | R342C | XP_011520919.1 |
XM_011522618.2 | 2258 | Intron | XP_011520920.1 | ||
XM_017023575.1 | 2258 | Intron | XP_016879064.1 | ||
XM_017023576.1 | 2258 | Missense Mutation | CGT,TGT | R481C | XP_016879065.1 |
XM_017023577.1 | 2258 | Missense Mutation | CGT,TGT | R426C | XP_016879066.1 |
XM_017023578.1 | 2258 | Missense Mutation | CGT,TGT | R347C | XP_016879067.1 |
XM_017023579.1 | 2258 | Missense Mutation | CGT,TGT | R342C | XP_016879068.1 |
XM_017023580.1 | 2258 | Missense Mutation | CGT,TGT | R342C | XP_016879069.1 |
XM_017023581.1 | 2258 | Intron | XP_016879070.1 |