ENST00000682431.1:n.1033+127T>G
|
|
|
ENST00000683018.1:c.697+127T>G
|
ENSP00000506822.1:n.697+127T>G
|
|
ENST00000683059.1:c.697+127T>G
|
ENSP00000507402.1:n.697+127T>G
|
|
ENST00000683164.1:c.697+127T>G
|
ENSP00000508051.1:n.697+127T>G
|
|
ENST00000683653.1:n.828+127T>G
|
|
|
ENST00000684500.1:n.1003+127T>G
|
|
|
ENST00000267101.8:c.874+127T>G
MANE Select
|
ENSP00000267101.4:n.874+127T>G
|
|
ENST00000267101.7:c.874+127T>G
|
ENSP00000267101.3:n.874+127T>G
|
|
ENST00000415288.6:c.697+127T>G
|
ENSP00000408340.2:n.697+127T>G
|
|
ENST00000546748.1:n.339+127T>G
|
|
|
ENST00000550869.5:c.25-6192T>G
|
ENSP00000448671.1:n.25-6192T>G
|
|
ENST00000551085.5:c.874+127T>G
|
ENSP00000448483.1:n.874+127T>G
|
|
ENST00000551242.5:c.874+127T>G
|
ENSP00000447510.1:n.874+127T>G
|
|
NM_001982.3:c.874+127T>G
|
NP_001973.2:n.874+127T>G
|
|
NM_001982.4:c.874+127T>G
MANE Select
|
NP_001973.2:n.874+127T>G
|
|