ENST00000411641.7:c.826G>T
MANE Select
|
ENSP00000393887.2:p.Asp276Tyr
|
|
ENST00000273784.5:c.829G>T
|
ENSP00000273784.5:p.Asp277Tyr
|
|
ENST00000411641.6:c.826G>T
|
ENSP00000393887.2:p.Asp276Tyr
|
|
NM_001622.2:c.826G>T
|
NP_001613.2:p.Asp276Tyr
|
|
NM_001354571.1:c.829G>T
|
NP_001341500.1:p.Asp277Tyr
|
|
NM_001354572.1:c.823G>T
|
NP_001341501.1:p.Asp275Tyr
|
|
NM_001354573.1:c.742G>T
|
NP_001341502.1:p.Asp248Tyr
|
|
NM_001622.3:c.826G>T
|
NP_001613.2:p.Asp276Tyr
|
|
NM_001622.4:c.826G>T
MANE Select
|
NP_001613.2:p.Asp276Tyr
|
|
NM_001354571.2:c.829G>T
|
NP_001341500.1:p.Asp277Tyr
|
|
NM_001354572.2:c.823G>T
|
NP_001341501.1:p.Asp275Tyr
|
|
NM_001354573.2:c.742G>T
|
NP_001341502.1:p.Asp248Tyr
|
|