|
NM_000975.5:c.508-2A>G
MANE Select
|
NP_000966.2:n.508-2A>G
|
|
ENST00000643754.2:c.508-2A>G
MANE Select
|
ENSP00000496250.1:n.508-2A>G
|
|
NM_000975.3:c.508-2A>G
|
NP_000966.2:n.508-2A>G
|
|
NM_001199802.1:c.505-2A>G
|
NP_001186731.1:n.505-2A>G
|
|
ENST00000374550.7:c.508-2A>G
|
ENSP00000363676.3:n.508-2A>G
|
|
ENST00000374550.8:c.505-2A>G
|
ENSP00000363676.4:n.505-2A>G
|
|
ENST00000443624.6:n.1532-2A>G
|
|
|
ENST00000458455.2:c.475-2A>G
|
ENSP00000398888.2:n.475-2A>G
|
|
ENST00000467075.2:c.*604-2A>G
|
ENSP00000493634.1:n.*604-2A>G
|
|
ENST00000482370.1:n.805-2A>G
|
|