ENST00000295754.10:c.454+5874T>G
MANE Select
|
ENSP00000295754.5:n.454+5874T>G
|
|
ENST00000672866.1:n.2050+5874T>G
|
|
|
ENST00000295754.9:c.454+5874T>G
|
ENSP00000295754.5:n.454+5874T>G
|
|
ENST00000359013.4:c.529+5874T>G
|
ENSP00000351905.4:n.529+5874T>G
|
|
NM_001024847.2:c.529+5874T>G , LRG_779t1:c.529+5874T>G
|
NP_001020018.1:n.529+5874T>G
|
|
NM_003242.5:c.454+5874T>G
|
NP_003233.4:n.454+5874T>G
|
|
XM_011534043.1:c.481+5874T>G
|
XP_011532345.1:n.481+5874T>G
|
|
XM_011534044.1:c.406+5874T>G
|
XP_011532346.1:n.406+5874T>G
|
|
XM_011534045.1:c.349+5874T>G
|
XP_011532347.1:n.349+5874T>G
|
|
XR_940692.1:n.2853T>G
|
|
|
XM_011534043.2:c.481+5874T>G
|
XP_011532345.1:n.481+5874T>G
|
|
XM_011534045.3:c.349+5874T>G
|
XP_011532347.1:n.349+5874T>G
|
|
XM_017007106.1:c.349+5874T>G
|
XP_016862595.1:n.349+5874T>G
|
|
XR_001740630.1:n.2355T>G
|
|
|
XR_001740631.1:n.647-1373T>G
|
|
|
NM_003242.6:c.454+5874T>G
MANE Select
|
NP_003233.4:n.454+5874T>G
|
|