|
NM_000975.5:c.397-2A>G
MANE Select
|
NP_000966.2:n.397-2A>G
|
|
ENST00000643754.2:c.397-2A>G
MANE Select
|
ENSP00000496250.1:n.397-2A>G
|
|
NM_000975.3:c.397-2A>G
|
NP_000966.2:n.397-2A>G
|
|
NM_001199802.1:c.394-2A>G
|
NP_001186731.1:n.394-2A>G
|
|
ENST00000374550.7:c.397-2A>G
|
ENSP00000363676.3:n.397-2A>G
|
|
ENST00000374550.8:c.394-2A>G
|
ENSP00000363676.4:n.394-2A>G
|
|
ENST00000443624.6:n.1419A>G
|
|
|
ENST00000458455.1:c.391-2A>G
|
ENSP00000398888.1:n.391-2A>G
|
|
ENST00000458455.2:c.364-2A>G
|
ENSP00000398888.2:n.364-2A>G
|
|
ENST00000467075.2:c.*493-2A>G
|
ENSP00000493634.1:n.*493-2A>G
|
|
ENST00000482370.1:n.694-2A>G
|
|
|
ENST00000482370.2:n.391-2A>G
|
|