ENST00000340855.11:c.1054G>T
MANE Select
|
ENSP00000339801.6:p.Asp352Tyr
|
|
ENST00000651111.1:c.421G>T
|
ENSP00000498395.1:p.Asp141Tyr
|
|
ENST00000340855.10:c.1054G>T
|
ENSP00000339801.6:p.Asp352Tyr
|
|
ENST00000422081.6:c.421G>T
|
ENSP00000477056.1:p.Asp141Tyr
|
|
ENST00000441880.1:n.161G>T
|
|
|
NM_000202.6:c.1054G>T
|
NP_000193.1:p.Asp352Tyr
|
|
NM_001166550.2:c.784G>T
|
NP_001160022.1:p.Asp262Tyr
|
|
NM_000202.7:c.1054G>T
|
NP_000193.1:p.Asp352Tyr
|
|
NM_001166550.3:c.784G>T
|
NP_001160022.1:p.Asp262Tyr
|
|
NM_000202.8:c.1054G>T
MANE Select
|
NP_000193.1:p.Asp352Tyr
|
|
NM_001166550.4:c.784G>T
|
NP_001160022.1:p.Asp262Tyr
|
|