ENST00000290866.10:c.3727G>A
MANE Select
|
ENSP00000290866.4:p.Val1243Ile
|
|
ENST00000290863.10:c.2005G>A
|
ENSP00000290863.6:p.Val669Ile
|
|
ENST00000290866.9:c.3727G>A
|
ENSP00000290866.4:p.Val1243Ile
|
|
ENST00000413513.7:c.1882G>A
|
ENSP00000392247.3:p.Val628Ile
|
|
ENST00000428043.5:c.*149G>A
|
ENSP00000397593.2:n.*149G>A
|
|
ENST00000577647.2:c.1969+187G>A
|
ENSP00000464149.1:n.1969+187G>A
|
|
ENST00000578839.5:c.*1482G>A
|
ENSP00000462110.2:n.*1482G>A
|
|
ENST00000579314.5:c.*1456G>A
|
ENSP00000462599.1:n.*1456G>A
|
|
NM_000789.3:c.3727G>A
|
NP_000780.1:p.Val1243Ile
|
|
NM_001178057.1:c.1882G>A
|
NP_001171528.1:p.Val628Ile
|
|
NM_152830.2:c.2005G>A
|
NP_690043.1:p.Val669Ile
|
|
XM_005257110.1:c.3178G>A
|
XP_005257167.1:p.Val1060Ile
|
|
XM_006721737.2:c.2065G>A
|
XP_006721800.2:p.Val689Ile
|
|
XM_006721737.3:c.2065G>A
|
XP_006721800.2:p.Val689Ile
|
|
NM_000789.4:c.3727G>A
MANE Select
|
NP_000780.1:p.Val1243Ile
|
|
NM_001178057.2:c.1882G>A
|
NP_001171528.1:p.Val628Ile
|
|
NM_152830.3:c.2005G>A
|
NP_690043.1:p.Val669Ile
|
|
NM_001382700.1:c.3160G>A
|
NP_001369629.1:p.Val1054Ile
|
|
NM_001382701.1:c.2875G>A
|
NP_001369630.1:p.Val959Ile
|
|
NM_001382702.1:c.1342G>A
|
NP_001369631.1:p.Val448Ile
|
|
NR_168483.1:n.2105G>A
|
|
|