ENST00000706645.1:n.1592+339A>G
|
|
|
ENST00000281243.10:c.545+339A>G
MANE Select
|
ENSP00000281243.5:n.545+339A>G
|
|
ENST00000281243.9:c.545+339A>G
|
ENSP00000281243.5:n.545+339A>G
|
|
ENST00000428702.6:c.452+339A>G
|
ENSP00000390944.2:n.452+339A>G
|
|
ENST00000501943.6:n.282+339A>G
|
|
|
ENST00000505710.1:c.364-1148A>G
|
|
|
ENST00000507439.5:c.437-1148A>G
|
ENSP00000423227.1:n.437-1148A>G
|
|
ENST00000508623.5:c.437-4657A>G
|
ENSP00000426377.1:n.437-4657A>G
|
|
ENST00000511609.1:n.277+339A>G
|
|
|
ENST00000513615.5:c.437-1148A>G
|
ENSP00000422759.1:n.437-1148A>G
|
|
ENST00000514300.1:c.*368-1148A>G
|
ENSP00000426039.1:n.*368-1148A>G
|
|
NM_000320.2:c.545+339A>G
|
NP_000311.2:n.545+339A>G
|
|
NM_001306140.1:c.452+339A>G
|
NP_001293069.1:n.452+339A>G
|
|
XR_241677.1:n.600-1148A>G
|
|
|
NR_156494.1:n.617-1148A>G
|
|
|
NM_000320.3:c.545+339A>G
MANE Select
|
NP_000311.2:n.545+339A>G
|
|
NM_001306140.2:c.452+339A>G
|
NP_001293069.1:n.452+339A>G
|
|
NR_156494.2:n.473-1148A>G
|
|
|