ENST00000697149.1:c.1571G>A
|
ENSP00000513138.1:n.1571G>A
|
|
ENST00000697150.1:c.1629G>A
|
ENSP00000513139.1:n.1629G>A
|
|
ENST00000697151.1:c.1562G>A
|
ENSP00000513140.1:n.1562G>A
|
|
ENST00000697164.1:c.1642G>A
|
ENSP00000513153.1:p.Asp548Asn
|
|
ENST00000697165.1:c.1429G>A
|
ENSP00000513154.1:p.Asp477Asn
|
|
ENST00000347310.10:c.1732G>A
MANE Select
|
ENSP00000321345.5:p.Asp578Asn
|
|
ENST00000637002.1:c.1123G>A
|
ENSP00000490340.1:p.Asp375Asn
|
|
ENST00000347310.9:c.1732G>A
|
ENSP00000321345.5:p.Asp578Asn
|
|
ENST00000395227.2:c.526G>A
|
ENSP00000378652.2:p.Asp176Asn
|
|
ENST00000425614.3:c.967G>A
|
ENSP00000387640.2:p.Asp323Asn
|
|
ENST00000473881.2:c.*558G>A
|
ENSP00000486667.1:n.*558G>A
|
|
NM_144701.2:c.1732G>A
|
NP_653302.2:p.Asp578Asn
|
|
XM_005270516.2:c.970G>A
|
XP_005270573.1:p.Asp324Asn
|
|
XM_011540789.1:c.1822G>A
|
XP_011539091.1:p.Asp608Asn
|
|
XM_011540790.1:c.1732G>A
|
XP_011539092.1:p.Asp578Asn
|
|
XM_011540791.1:c.1732G>A
|
XP_011539093.1:p.Asp578Asn
|
|
XM_011540790.3:c.1732G>A
|
XP_011539092.1:p.Asp578Asn
|
|
XM_011540791.3:c.1732G>A
|
XP_011539093.1:p.Asp578Asn
|
|
XR_001736993.1:n.1812G>A
|
|
|
NM_144701.3:c.1732G>A
MANE Select
|
NP_653302.2:p.Asp578Asn
|
|