ENST00000290866.10:c.3380+823C>T
MANE Select
|
ENSP00000290866.4:n.3380+823C>T
|
|
ENST00000290863.10:c.1658+823C>T
|
ENSP00000290863.6:n.1658+823C>T
|
|
ENST00000290866.9:c.3380+823C>T
|
ENSP00000290866.4:n.3380+823C>T
|
|
ENST00000413513.7:c.1658+823C>T
|
ENSP00000392247.3:n.1658+823C>T
|
|
ENST00000428043.5:c.3380+823C>T
|
ENSP00000397593.2:n.3380+823C>T
|
|
ENST00000577418.5:n.390+823C>T
|
|
|
ENST00000577647.2:c.1658+823C>T
|
ENSP00000464149.1:n.1658+823C>T
|
|
ENST00000578839.5:c.*1258+823C>T
|
ENSP00000462110.2:n.*1258+823C>T
|
|
ENST00000579314.5:c.*1109+823C>T
|
ENSP00000462599.1:n.*1109+823C>T
|
|
ENST00000579409.1:c.67+823C>T
|
|
|
NM_000789.3:c.3380+823C>T
|
NP_000780.1:n.3380+823C>T
|
|
NM_001178057.1:c.1658+823C>T
|
NP_001171528.1:n.1658+823C>T
|
|
NM_152830.2:c.1658+823C>T
|
NP_690043.1:n.1658+823C>T
|
|
XM_005257110.1:c.2831+823C>T
|
XP_005257167.1:n.2831+823C>T
|
|
XM_006721737.2:c.1718+823C>T
|
XP_006721800.2:n.1718+823C>T
|
|
XM_006721737.3:c.1718+823C>T
|
XP_006721800.2:n.1718+823C>T
|
|
NM_000789.4:c.3380+823C>T
MANE Select
|
NP_000780.1:n.3380+823C>T
|
|
NM_001178057.2:c.1658+823C>T
|
NP_001171528.1:n.1658+823C>T
|
|
NM_152830.3:c.1658+823C>T
|
NP_690043.1:n.1658+823C>T
|
|
NM_001382700.1:c.2813+823C>T
|
NP_001369629.1:n.2813+823C>T
|
|
NM_001382701.1:c.2528+823C>T
|
NP_001369630.1:n.2528+823C>T
|
|
NM_001382702.1:c.1118+823C>T
|
NP_001369631.1:n.1118+823C>T
|
|
NR_168483.1:n.1758+823C>T
|
|
|