ENST00000559133.6:c.5789-151A>G
|
ENSP00000453958.2:n.5789-151A>G
|
|
ENST00000674301.2:c.5789-151A>G
|
ENSP00000501333.2:n.5789-151A>G
|
|
ENST00000684448.1:n.4463-151A>G
|
|
|
ENST00000316623.10:c.5789-151A>G
MANE Select
|
ENSP00000325527.5:n.5789-151A>G
|
|
ENST00000674301.1:c.788-151A>G
|
ENSP00000501333.1:n.788-151A>G
|
|
ENST00000316623.9:c.5789-151A>G
|
ENSP00000325527.5:n.5789-151A>G
|
|
ENST00000537463.6:c.*1552-151A>G
|
ENSP00000440294.2:n.*1552-151A>G
|
|
ENST00000559133.5:c.1096-151A>G
|
|
|
NM_000138.4:c.5789-151A>G , LRG_778t1:c.5789-151A>G
|
NP_000129.3:n.5789-151A>G
|
|
NM_000138.5:c.5789-151A>G
MANE Select
|
NP_000129.3:n.5789-151A>G
|
|