Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_134268.4 | 321 | Missense Mutation | TCT,TGT | S104C | NP_599030.1 |
XM_005257005.2 | 321 | Missense Mutation | TCT,TGT | S104C | XP_005257062.1 |
XM_017024116.1 | 321 | Missense Mutation | TCT,TGT | S39C | XP_016879605.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077620.2 | 321 | Intron | NP_001071088.1 | ||
XM_017025013.1 | 321 | Intron | XP_016880502.1 | ||
XM_017025014.1 | 321 | Intron | XP_016880503.1 | ||
XM_017025015.1 | 321 | Intron | XP_016880504.1 |