ENST00000257749.9:c.*1276C>A
MANE Select
|
ENSP00000257749.4:n.*1276C>A
|
|
ENST00000257749.8:c.*1276C>A
|
ENSP00000257749.4:n.*1276C>A
|
|
ENST00000537989.5:c.*1276C>A
|
ENSP00000437473.1:n.*1276C>A
|
|
NM_001170794.1:c.*1276C>A
|
NP_001164265.1:n.*1276C>A
|
|
NM_021813.3:c.*1276C>A
|
NP_068585.1:n.*1276C>A
|
|
XM_005248758.3:c.*1276C>A
|
XP_005248815.1:n.*1276C>A
|
|
XM_005248759.3:c.*1276C>A
|
XP_005248816.1:n.*1276C>A
|
|
XM_011536037.1:c.*1276C>A
|
XP_011534339.1:n.*1276C>A
|
|
XM_011536038.1:c.*1276C>A
|
XP_011534340.1:n.*1276C>A
|
|
XM_011536039.1:c.*1276C>A
|
XP_011534341.1:n.*1276C>A
|
|
XM_011536040.1:c.*1276C>A
|
XP_011534342.1:n.*1276C>A
|
|
XM_011536041.1:c.*1276C>A
|
XP_011534343.1:n.*1276C>A
|
|
XM_005248758.5:c.*1276C>A
|
XP_005248815.1:n.*1276C>A
|
|
XM_005248759.5:c.*1276C>A
|
XP_005248816.1:n.*1276C>A
|
|
XM_017011166.2:c.*1276C>A
|
XP_016866655.1:n.*1276C>A
|
|
XM_024446510.1:c.*1276C>A
|
XP_024302278.1:n.*1276C>A
|
|
XM_024446511.1:c.*1276C>A
|
XP_024302279.1:n.*1276C>A
|
|
NM_021813.4:c.*1276C>A
MANE Select
|
NP_068585.1:n.*1276C>A
|
|
NM_001170794.2:c.*1276C>A
|
NP_001164265.1:n.*1276C>A
|
|