ENST00000396623.8:c.1029T>G
MANE Select
|
ENSP00000379865.3:p.Tyr343Ter
|
|
ENST00000648156.1:c.*248T>G
|
ENSP00000497007.1:n.*248T>G
|
|
ENST00000276576.11:c.*865T>G
|
ENSP00000276576.7:n.*865T>G
|
|
ENST00000396623.7:c.1029T>G
|
ENSP00000379865.3:p.Tyr343Ter
|
|
ENST00000415254.5:c.885T>G
|
ENSP00000407115.1:p.Tyr295Ter
|
|
ENST00000419955.5:c.*1038T>G
|
ENSP00000392040.1:n.*1038T>G
|
|
ENST00000424777.6:c.*466T>G
|
ENSP00000410883.2:n.*466T>G
|
|
ENST00000426810.5:c.*1214T>G
|
ENSP00000406905.1:n.*1214T>G
|
|
ENST00000480040.5:n.104T>G
|
|
|
ENST00000496501.5:n.903T>G
|
|
|
NM_144650.2:c.1029T>G
|
NP_653251.2:p.Tyr343Ter
|
|
NM_144650.3:c.1029T>G
MANE Select
|
NP_653251.2:p.Tyr343Ter
|
|