Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001184935.1 | 1040 | Missense Mutation | CGC,TGC | R518C | NP_001171864.1 |
NM_004883.2 | 1040 | Missense Mutation | CGC,TGC | R584C | NP_004874.1 |
NM_013981.3 | 1040 | Missense Mutation | CGC,TGC | R578C | NP_053584.1 |
NM_013982.2 | 1040 | Missense Mutation | CGC,TGC | R592C | NP_053585.1 |
NM_013983.2 | 1040 | Missense Mutation | CGC,TGC | R586C | NP_053586.1 |
XM_005268533.3 | 1040 | Missense Mutation | CGC,TGC | R193C | XP_005268590.1 |
XM_006714810.3 | 1040 | Intron | XP_006714873.1 | ||
XM_011537713.2 | 1040 | Intron | XP_011536015.1 | ||
XM_017010064.1 | 1040 | Missense Mutation | CGC,TGC | R204C | XP_016865553.1 |
XM_017010065.1 | 1040 | Missense Mutation | CGC,TGC | R201C | XP_016865554.1 |
XM_017010066.1 | 1040 | Intron | XP_016865555.1 |