Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001255978.1 | 402 | Missense Mutation | CCA,CTA | P35L | NP_001242907.1 |
NM_001255979.1 | 402 | Missense Mutation | CCA,CTA | P35L | NP_001242908.1 |
NM_001255980.1 | 402 | Missense Mutation | CCA,CTA | P35L | NP_001242909.1 |
NM_001255981.1 | 402 | Missense Mutation | CCA,CTA | P35L | NP_001242910.1 |
NM_130898.3 | 402 | Missense Mutation | CCA,CTA | P35L | NP_570968.1 |
XM_006711172.2 | 402 | Missense Mutation | CCA,CTA | P35L | XP_006711235.1 |
XM_017000372.1 | 402 | Missense Mutation | CCA,CTA | P35L | XP_016855861.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271957.1 | 402 | Intron | NP_001258886.1 | ||
NM_001271958.1 | 402 | Intron | NP_001258887.1 | ||
NM_001271959.1 | 402 | Intron | NP_001258888.1 | ||
NM_001271960.1 | 402 | Intron | NP_001258889.1 | ||
NM_001271961.1 | 402 | Intron | NP_001258890.1 | ||
NM_014437.4 | 402 | Intron | NP_055252.2 |