ENST00000334398.8:c.995+987C>A
MANE Select
|
ENSP00000335261.3:n.995+987C>A
|
|
ENST00000675642.1:c.1028+987C>A
|
ENSP00000502604.1:n.1028+987C>A
|
|
ENST00000334398.7:c.995+987C>A
|
ENSP00000335261.3:n.995+987C>A
|
|
ENST00000369439.4:c.995+987C>A
|
ENSP00000358447.4:n.995+987C>A
|
|
NM_001184797.1:c.995+987C>A
|
NP_001171726.1:n.995+987C>A
|
|
NM_018196.3:c.995+987C>A
|
NP_060666.1:n.995+987C>A
|
|
XM_011531182.1:c.842+987C>A
|
XP_011529484.1:n.842+987C>A
|
|
XR_247318.1:n.1166+987C>A
|
|
|
XM_011531182.3:c.842+987C>A
|
XP_011529484.1:n.842+987C>A
|
|
XR_247318.3:n.1140+987C>A
|
|
|
NM_018196.4:c.995+987C>A
MANE Select
|
NP_060666.1:n.995+987C>A
|
|
NM_001184797.2:c.995+987C>A
|
NP_001171726.1:n.995+987C>A
|
|