ENST00000587656.6:c.2719-29G>A
|
ENSP00000468638.2:n.2719-29G>A
|
|
ENST00000294618.12:c.2718+885G>A
MANE Select
|
ENSP00000294618.6:n.2718+885G>A
|
|
ENST00000294618.11:c.2718+885G>A
|
ENSP00000294618.6:n.2718+885G>A
|
|
ENST00000585904.1:c.322-29G>A
|
ENSP00000465767.1:n.322-29G>A
|
|
ENST00000587656.5:c.479-29G>A
|
|
|
ENST00000590680.5:c.1061+885G>A
|
|
|
NM_020812.3:c.2718+885G>A
|
NP_065863.2:n.2718+885G>A
|
|
XM_005260000.2:c.2719-29G>A
|
XP_005260057.1:n.2719-29G>A
|
|
XM_005260001.2:c.2719-29G>A
|
XP_005260058.1:n.2719-29G>A
|
|
XM_006722804.2:c.54+721G>A
|
XP_006722867.1:n.54+721G>A
|
|
XM_011528150.1:c.2752-29G>A
|
XP_011526452.1:n.2752-29G>A
|
|
XM_011528151.1:c.2751+885G>A
|
XP_011526453.1:n.2751+885G>A
|
|
XM_011528152.1:c.2751+885G>A
|
XP_011526454.1:n.2751+885G>A
|
|
XM_011528153.1:c.2752-29G>A
|
XP_011526455.1:n.2752-29G>A
|
|
XR_936195.1:n.2813-29G>A
|
|
|
XR_936196.1:n.2812+885G>A
|
|
|
XR_936197.1:n.2813-29G>A
|
|
|
XR_936198.1:n.2812+885G>A
|
|
|
XM_006722804.3:c.54+721G>A
|
XP_006722867.1:n.54+721G>A
|
|
NM_001367830.1:c.2719-29G>A
|
NP_001354759.1:n.2719-29G>A
|
|
NM_020812.4:c.2718+885G>A
MANE Select
|
NP_065863.2:n.2718+885G>A
|
|