Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318798.1 | 190 | Intron | NP_001305727.1 | ||
NM_001318800.1 | 190 | Missense Mutation | CCC,TCC | P19S | NP_001305729.1 |
NM_004186.4 | 190 | Missense Mutation | CCC,TCC | P19S | NP_004177.3 |
XM_005265381.4 | 190 | Missense Mutation | CCC,TCC | P19S | XP_005265438.1 |
XM_005265382.4 | 190 | Missense Mutation | CCC,TCC | P19S | XP_005265439.1 |
XM_006713289.3 | 190 | Intron | XP_006713352.1 | ||
XM_006713290.3 | 190 | Missense Mutation | CCC,TCC | P19S | XP_006713353.1 |
XM_011533998.2 | 190 | Missense Mutation | CCC,TCC | P19S | XP_011532300.1 |
XM_011534000.2 | 190 | Missense Mutation | CCC,TCC | P19S | XP_011532302.1 |