NM_022765.4:c.2787+12G>A
MANE Select
|
NP_073602.3:n.2787+12G>A
|
ENST00000358807.8:c.2787+12G>A
MANE Select
|
ENSP00000351664.3:n.2787+12G>A
|
NM_001159291.1:c.2529+12G>A
|
NP_001152763.1:n.2529+12G>A
|
NM_001159291.2:c.2529+12G>A
|
NP_001152763.1:n.2529+12G>A
|
NM_001286613.1:c.2844+12G>A
|
NP_001273542.1:n.2844+12G>A
|
NM_001286613.2:c.2844+12G>A
|
NP_001273542.1:n.2844+12G>A
|
NM_022765.3:c.2787+12G>A
|
NP_073602.3:n.2787+12G>A
|
ENST00000358577.7:c.2529+12G>A
|
ENSP00000351385.3:n.2529+12G>A
|
ENST00000358807.7:c.2787+12G>A
|
ENSP00000351664.3:n.2787+12G>A
|
ENST00000456101.6:n.3566+12G>A
|
|
ENST00000465904.1:n.3838+12G>A
|
|
ENST00000630715.2:c.2844+12G>A
|
ENSP00000486901.1:n.2844+12G>A
|