|
ENST00000371418.9:c.1128G>A
MANE Select
|
ENSP00000360472.4:p.Trp376Ter
|
|
|
ENST00000485458.3:n.5104G>A
|
|
|
|
ENST00000635804.1:n.562G>A
|
|
|
|
ENST00000635953.1:c.*550G>A
|
ENSP00000490058.1:n.*550G>A
|
|
|
ENST00000636155.1:c.838+3907G>A
|
ENSP00000490355.1:n.838+3907G>A
|
|
|
ENST00000636232.1:c.*914G>A
|
ENSP00000490325.1:n.*914G>A
|
|
|
ENST00000636754.1:c.*970G>A
|
ENSP00000489781.1:n.*970G>A
|
|
|
ENST00000636946.1:c.*1008-492G>A
|
ENSP00000490654.1:n.*1008-492G>A
|
|
|
ENST00000637037.1:c.*718G>A
|
ENSP00000490860.1:n.*718G>A
|
|
|
ENST00000637347.1:n.989G>A
|
|
|
|
ENST00000637611.1:c.*684G>A
|
ENSP00000489682.1:n.*684G>A
|
|
|
ENST00000637689.1:c.-244G>A
|
ENSP00000490496.1:n.-244G>A
|
|
|
ENST00000637925.1:c.*723G>A
|
ENSP00000489763.1:n.*723G>A
|
|
|
ENST00000638049.1:c.*886G>A
|
ENSP00000490597.1:n.*886G>A
|
|
|
ENST00000676175.1:n.2867G>A
|
|
|
|
ENST00000371413.4:c.839-492G>A
|
ENSP00000360467.3:n.839-492G>A
|
|
|
ENST00000371418.8:c.1128G>A
|
ENSP00000360472.4:p.Trp376Ter
|
|
|
ENST00000626307.1:n.5043G>A
|
|
|
|
ENST00000627420.2:c.*837G>A
|
ENSP00000487116.1:n.*837G>A
|
|
|
ENST00000629035.2:c.1056G>A
|
ENSP00000486908.1:p.Trp352Ter
|
|
|
ENST00000630047.2:c.984G>A
|
ENSP00000485917.1:p.Trp328Ter
|
|
|
NM_001308275.1:c.839-492G>A
|
NP_001295204.1:n.839-492G>A
|
|
|
NM_001308276.1:c.984G>A
|
NP_001295205.1:p.Trp328Ter
|
|
|
NM_005097.2:c.1128G>A
|
NP_005088.1:p.Trp376Ter
|
|
|
NM_005097.3:c.1128G>A
|
NP_005088.1:p.Trp376Ter
|
|
|
NR_131777.1:n.1392G>A
|
|
|
|
XM_017016912.2:c.695-492G>A
|
XP_016872401.1:n.695-492G>A
|
|
|
NM_005097.4:c.1128G>A
MANE Select
|
NP_005088.1:p.Trp376Ter
|
|
|
NM_001308275.2:c.839-492G>A
|
NP_001295204.1:n.839-492G>A
|
|
|
NM_001308276.2:c.984G>A
|
NP_001295205.1:p.Trp328Ter
|
|
|
NR_131777.2:n.1265G>A
|
|
|
