|
ENST00000696202.1:n.501G>T
(COPA)
|
|
|
|
ENST00000696203.1:n.3313G>T
(COPA)
|
|
|
|
ENST00000696204.1:n.3520G>T
(COPA)
|
|
|
|
ENST00000696206.1:n.600G>T
(COPA)
|
|
|
|
ENST00000696207.1:n.826G>T
(COPA)
|
|
|
|
ENST00000696208.1:n.932G>T
(COPA)
|
|
|
|
ENST00000696209.1:n.1225G>T
(COPA)
|
|
|
|
ENST00000696210.1:n.1225G>T
(COPA)
|
|
|
|
ENST00000696211.1:n.1225G>T
(COPA)
|
|
|
|
ENST00000696212.1:n.3513G>T
(COPA)
|
|
|
|
ENST00000696213.1:n.1956G>T
(COPA)
|
|
|
|
ENST00000696214.1:n.3539G>T
(COPA)
|
|
|
|
ENST00000696215.1:n.932G>T
(COPA)
|
|
|
|
ENST00000241704.8:c.829G>T
(COPA)
MANE Select
|
ENSP00000241704.7:p.Asp277Tyr
|
|
|
ENST00000647683.1:c.829G>T
(COPA)
|
ENSP00000497495.1:p.Asp277Tyr
|
|
|
ENST00000647693.1:n.1913G>T
(COPA)
|
|
|
|
ENST00000647799.1:c.*266G>T
(COPA)
|
ENSP00000497970.1:n.*266G>T
|
|
|
ENST00000647899.1:c.348G>T
(COPA)
|
|
|
|
ENST00000648501.1:c.316-836G>T
(COPA)
|
|
|
|
ENST00000648805.1:c.829G>T
(COPA)
|
ENSP00000497433.1:p.Asp277Tyr
|
|
|
ENST00000649231.1:c.829G>T
(COPA)
|
ENSP00000498061.1:p.Asp277Tyr
|
|
|
ENST00000649676.1:c.376G>T
(COPA)
|
ENSP00000497257.1:p.Asp126Tyr
|
|
|
ENST00000649787.1:c.829G>T
(COPA)
|
ENSP00000497231.1:p.Asp277Tyr
|
|
|
ENST00000649963.1:c.*518G>T
(COPA)
|
ENSP00000498129.1:n.*518G>T
|
|
|
ENST00000650154.1:c.*266G>T
(COPA)
|
ENSP00000497094.1:n.*266G>T
|
|
|
ENST00000241704.7:c.829G>T
(COPA)
|
ENSP00000241704.7:p.Asp277Tyr
|
|
|
ENST00000368069.7:c.829G>T
(COPA)
|
ENSP00000357048.3:p.Asp277Tyr
|
|
|
NM_001098398.1:c.829G>T
(COPA)
|
NP_001091868.1:p.Asp277Tyr
|
|
|
NM_004371.3:c.829G>T
(COPA)
|
NP_004362.2:p.Asp277Tyr
|
|
|
XM_011509584.1:c.-176+27412C>A
(NHLH1)
|
XP_011507886.1:n.-176+27412C>A
|
|
|
NM_001098398.2:c.829G>T
(COPA)
|
NP_001091868.1:p.Asp277Tyr
|
|
|
NM_004371.4:c.829G>T
(COPA)
MANE Select
|
NP_004362.2:p.Asp277Tyr
|
|
