Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142391.2 | 1674 | Missense Mutation | GCC,GTC | A402V | NP_001135863.1 |
NM_001142392.2 | 1674 | Missense Mutation | GCC,GTC | A431V | NP_001135864.1 |
NM_019848.4 | 1674 | Missense Mutation | GCC,GTC | A431V | NP_062822.1 |
XM_005277913.4 | 1674 | Missense Mutation | GCC,GTC | A486V | XP_005277970.1 |
XM_006724847.3 | 1674 | Missense Mutation | GCC,GTC | A524V | XP_006724910.1 |
XM_006724848.3 | 1674 | Missense Mutation | GCC,GTC | A495V | XP_006724911.1 |
XM_011531200.2 | 1674 | Missense Mutation | GCC,GTC | A486V | XP_011529502.2 |
XM_011531201.2 | 1674 | Missense Mutation | GCC,GTC | A431V | XP_011529503.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014235.4 | 1674 | Intron | NP_055050.1 |