|
ENST00000371418.9:c.838+115A>G
MANE Select
|
ENSP00000360472.4:n.838+115A>G
|
|
|
ENST00000485458.3:n.4814+115A>G
|
|
|
|
ENST00000635953.1:c.838+115A>G
|
ENSP00000490058.1:n.838+115A>G
|
|
|
ENST00000636155.1:c.838+115A>G
|
ENSP00000490355.1:n.838+115A>G
|
|
|
ENST00000636232.1:c.*624+115A>G
|
ENSP00000490325.1:n.*624+115A>G
|
|
|
ENST00000636754.1:c.*680+115A>G
|
ENSP00000489781.1:n.*680+115A>G
|
|
|
ENST00000636946.1:c.*1007+115A>G
|
ENSP00000490654.1:n.*1007+115A>G
|
|
|
ENST00000637037.1:c.*428+115A>G
|
ENSP00000490860.1:n.*428+115A>G
|
|
|
ENST00000637347.1:n.699+115A>G
|
|
|
|
ENST00000637611.1:c.*394+115A>G
|
ENSP00000489682.1:n.*394+115A>G
|
|
|
ENST00000637689.1:c.-534+115A>G
|
ENSP00000490496.1:n.-534+115A>G
|
|
|
ENST00000637925.1:c.*433+115A>G
|
ENSP00000489763.1:n.*433+115A>G
|
|
|
ENST00000638049.1:c.*596+115A>G
|
ENSP00000490597.1:n.*596+115A>G
|
|
|
ENST00000676175.1:n.2577+115A>G
|
|
|
|
ENST00000371413.4:c.838+115A>G
|
ENSP00000360467.3:n.838+115A>G
|
|
|
ENST00000371418.8:c.838+115A>G
|
ENSP00000360472.4:n.838+115A>G
|
|
|
ENST00000626307.1:n.4753+115A>G
|
|
|
|
ENST00000626946.1:n.508+115A>G
|
|
|
|
ENST00000627420.2:c.*547+115A>G
|
ENSP00000487116.1:n.*547+115A>G
|
|
|
ENST00000629035.2:c.766+115A>G
|
ENSP00000486908.1:n.766+115A>G
|
|
|
ENST00000630047.2:c.694+115A>G
|
ENSP00000485917.1:n.694+115A>G
|
|
|
NM_001308275.1:c.838+115A>G
|
NP_001295204.1:n.838+115A>G
|
|
|
NM_001308276.1:c.694+115A>G
|
NP_001295205.1:n.694+115A>G
|
|
|
NM_005097.2:c.838+115A>G
|
NP_005088.1:n.838+115A>G
|
|
|
NM_005097.3:c.838+115A>G
|
NP_005088.1:n.838+115A>G
|
|
|
NR_131777.1:n.1102+115A>G
|
|
|
|
XM_017016911.2:c.838+115A>G
|
XP_016872400.1:n.838+115A>G
|
|
|
XM_017016912.2:c.694+115A>G
|
XP_016872401.1:n.694+115A>G
|
|
|
NM_005097.4:c.838+115A>G
MANE Select
|
NP_005088.1:n.838+115A>G
|
|
|
NM_001308275.2:c.838+115A>G
|
NP_001295204.1:n.838+115A>G
|
|
|
NM_001308276.2:c.694+115A>G
|
NP_001295205.1:n.694+115A>G
|
|
|
NR_131777.2:n.975+115A>G
|
|
|
