|
ENST00000696202.1:n.456G>C
(COPA)
|
|
|
|
ENST00000696203.1:n.3268G>C
(COPA)
|
|
|
|
ENST00000696204.1:n.3475G>C
(COPA)
|
|
|
|
ENST00000696206.1:n.555G>C
(COPA)
|
|
|
|
ENST00000696207.1:n.781G>C
(COPA)
|
|
|
|
ENST00000696208.1:n.887G>C
(COPA)
|
|
|
|
ENST00000696209.1:n.1180G>C
(COPA)
|
|
|
|
ENST00000696210.1:n.1180G>C
(COPA)
|
|
|
|
ENST00000696211.1:n.1180G>C
(COPA)
|
|
|
|
ENST00000696212.1:n.3468G>C
(COPA)
|
|
|
|
ENST00000696213.1:n.1911G>C
(COPA)
|
|
|
|
ENST00000696214.1:n.3494G>C
(COPA)
|
|
|
|
ENST00000696215.1:n.887G>C
(COPA)
|
|
|
|
ENST00000241704.8:c.784G>C
(COPA)
MANE Select
|
ENSP00000241704.7:p.Glu262Gln
|
|
|
ENST00000647683.1:c.784G>C
(COPA)
|
ENSP00000497495.1:p.Glu262Gln
|
|
|
ENST00000647693.1:n.1868G>C
(COPA)
|
|
|
|
ENST00000647799.1:c.*221G>C
(COPA)
|
ENSP00000497970.1:n.*221G>C
|
|
|
ENST00000647899.1:c.303G>C
(COPA)
|
|
|
|
ENST00000648501.1:c.316-881G>C
(COPA)
|
|
|
|
ENST00000648805.1:c.784G>C
(COPA)
|
ENSP00000497433.1:p.Glu262Gln
|
|
|
ENST00000649231.1:c.784G>C
(COPA)
|
ENSP00000498061.1:p.Glu262Gln
|
|
|
ENST00000649676.1:c.331G>C
(COPA)
|
ENSP00000497257.1:p.Glu111Gln
|
|
|
ENST00000649787.1:c.784G>C
(COPA)
|
ENSP00000497231.1:p.Glu262Gln
|
|
|
ENST00000649963.1:c.*473G>C
(COPA)
|
ENSP00000498129.1:n.*473G>C
|
|
|
ENST00000650154.1:c.*221G>C
(COPA)
|
ENSP00000497094.1:n.*221G>C
|
|
|
ENST00000241704.7:c.784G>C
(COPA)
|
ENSP00000241704.7:p.Glu262Gln
|
|
|
ENST00000368069.7:c.784G>C
(COPA)
|
ENSP00000357048.3:p.Glu262Gln
|
|
|
NM_001098398.1:c.784G>C
(COPA)
|
NP_001091868.1:p.Glu262Gln
|
|
|
NM_004371.3:c.784G>C
(COPA)
|
NP_004362.2:p.Glu262Gln
|
|
|
XM_011509584.1:c.-176+27457C>G
(NHLH1)
|
XP_011507886.1:n.-176+27457C>G
|
|
|
NM_001098398.2:c.784G>C
(COPA)
|
NP_001091868.1:p.Glu262Gln
|
|
|
NM_004371.4:c.784G>C
(COPA)
MANE Select
|
NP_004362.2:p.Glu262Gln
|
|
