ENST00000349243.8:c.*4G>A
MANE Select
|
ENSP00000273430.3:n.*4G>A
|
|
ENST00000402260.2:c.*4G>A
|
ENSP00000385641.3:n.*4G>A
|
|
ENST00000418473.7:c.*4G>A
|
ENSP00000398832.4:n.*4G>A
|
|
ENST00000349243.7:c.*4G>A
|
ENSP00000273430.3:n.*4G>A
|
|
ENST00000402260.1:c.*4G>A
|
ENSP00000385641.2:n.*4G>A
|
|
ENST00000404754.2:c.*4G>A
|
ENSP00000385612.2:n.*4G>A
|
|
ENST00000418473.6:c.1189G>A
|
ENSP00000398832.3:n.1189G>A
|
|
ENST00000461609.1:c.*4G>A
|
ENSP00000418851.1:n.*4G>A
|
|
ENST00000474935.5:c.*4G>A
|
ENSP00000418084.1:n.*4G>A
|
|
ENST00000475347.5:c.*4G>A
|
ENSP00000419783.1:n.*4G>A
|
|
ENST00000497524.5:c.*4G>A
|
ENSP00000419422.1:n.*4G>A
|
|
NM_000685.4:c.*4G>A
|
NP_000676.1:n.*4G>A
|
|
NM_004835.4:c.*4G>A
|
NP_004826.5:n.*4G>A
|
|
NM_009585.3:c.*4G>A
|
NP_033611.1:n.*4G>A
|
|
NM_031850.3:c.*4G>A
|
NP_114038.4:n.*4G>A
|
|
NM_032049.3:c.*4G>A
|
NP_114438.2:n.*4G>A
|
|
NM_000685.5:c.*4G>A
MANE Select
|
NP_000676.1:n.*4G>A
|
|
NM_001382736.1:c.*4G>A
|
NP_001369665.1:n.*4G>A
|
|
NM_001382737.1:c.*4G>A
|
NP_001369666.1:n.*4G>A
|
|
NM_004835.5:c.*4G>A
|
NP_004826.6:n.*4G>A
|
|
NM_009585.4:c.*4G>A
|
NP_033611.1:n.*4G>A
|
|
NM_031850.4:c.*4G>A
|
NP_114038.5:n.*4G>A
|
|
NM_032049.4:c.*4G>A
|
NP_114438.3:n.*4G>A
|
|