|
NM_000975.5:c.396+9A>G
MANE Select
|
NP_000966.2:n.396+9A>G
|
|
ENST00000643754.2:c.396+9A>G
MANE Select
|
ENSP00000496250.1:n.396+9A>G
|
|
NM_000975.3:c.396+9A>G
|
NP_000966.2:n.396+9A>G
|
|
NM_001199802.1:c.393+9A>G
|
NP_001186731.1:n.393+9A>G
|
|
ENST00000374550.7:c.396+9A>G
|
ENSP00000363676.3:n.396+9A>G
|
|
ENST00000374550.8:c.393+9A>G
|
ENSP00000363676.4:n.393+9A>G
|
|
ENST00000443624.5:c.399A>G
|
ENSP00000390839.1:n.399A>G
|
|
ENST00000443624.6:n.423A>G
|
|
|
ENST00000458455.1:c.390+9A>G
|
ENSP00000398888.1:n.390+9A>G
|
|
ENST00000458455.2:c.363+9A>G
|
ENSP00000398888.2:n.363+9A>G
|
|
ENST00000467075.2:c.*492+9A>G
|
ENSP00000493634.1:n.*492+9A>G
|
|
ENST00000482370.1:n.693+9A>G
|
|
|
ENST00000482370.2:n.390+9A>G
|
|