ENST00000290866.10:c.3710T>G
MANE Select
|
ENSP00000290866.4:p.Leu1237Arg
|
|
ENST00000290863.10:c.1988T>G
|
ENSP00000290863.6:p.Leu663Arg
|
|
ENST00000290866.9:c.3710T>G
|
ENSP00000290866.4:p.Leu1237Arg
|
|
ENST00000413513.7:c.1865T>G
|
ENSP00000392247.3:p.Leu622Arg
|
|
ENST00000428043.5:c.*132T>G
|
ENSP00000397593.2:n.*132T>G
|
|
ENST00000577418.5:n.720T>G
|
|
|
ENST00000577647.2:c.1969+170T>G
|
ENSP00000464149.1:n.1969+170T>G
|
|
ENST00000578839.5:c.*1465T>G
|
ENSP00000462110.2:n.*1465T>G
|
|
ENST00000579314.5:c.*1439T>G
|
ENSP00000462599.1:n.*1439T>G
|
|
NM_000789.3:c.3710T>G
|
NP_000780.1:p.Leu1237Arg
|
|
NM_001178057.1:c.1865T>G
|
NP_001171528.1:p.Leu622Arg
|
|
NM_152830.2:c.1988T>G
|
NP_690043.1:p.Leu663Arg
|
|
XM_005257110.1:c.3161T>G
|
XP_005257167.1:p.Leu1054Arg
|
|
XM_006721737.2:c.2048T>G
|
XP_006721800.2:p.Leu683Arg
|
|
XM_006721737.3:c.2048T>G
|
XP_006721800.2:p.Leu683Arg
|
|
NM_000789.4:c.3710T>G
MANE Select
|
NP_000780.1:p.Leu1237Arg
|
|
NM_001178057.2:c.1865T>G
|
NP_001171528.1:p.Leu622Arg
|
|
NM_152830.3:c.1988T>G
|
NP_690043.1:p.Leu663Arg
|
|
NM_001382700.1:c.3143T>G
|
NP_001369629.1:p.Leu1048Arg
|
|
NM_001382701.1:c.2858T>G
|
NP_001369630.1:p.Leu953Arg
|
|
NM_001382702.1:c.1325T>G
|
NP_001369631.1:p.Leu442Arg
|
|
NR_168483.1:n.2088T>G
|
|
|