ENST00000304874.14:c.829T>G
MANE Select
|
ENSP00000307188.9:p.Tyr277Asp
|
|
ENST00000362000.10:c.634T>G
|
ENSP00000354710.6:p.Tyr212Asp
|
|
ENST00000380839.9:c.751T>G
|
ENSP00000370219.4:p.Tyr251Asp
|
|
ENST00000395331.4:c.829T>G
|
ENSP00000378740.3:p.Tyr277Asp
|
|
ENST00000395332.8:c.829T>G
|
ENSP00000378741.3:p.Tyr277Asp
|
|
ENST00000671817.1:c.751T>G
|
ENSP00000500462.1:p.Tyr251Asp
|
|
ENST00000672498.1:c.*128T>G
|
ENSP00000500227.1:n.*128T>G
|
|
ENST00000672586.1:n.1588T>G
|
|
|
ENST00000672676.1:n.1853T>G
|
|
|
ENST00000673149.1:n.641T>G
|
|
|
ENST00000673350.1:n.2946T>G
|
|
|
ENST00000673518.1:c.751T>G
|
ENSP00000499889.1:p.Tyr251Asp
|
|
ENST00000304874.13:c.829T>G
|
ENSP00000307188.9:p.Tyr277Asp
|
|
ENST00000362000.9:c.634T>G
|
ENSP00000354710.5:p.Tyr212Asp
|
|
ENST00000380839.8:c.751T>G
|
ENSP00000370219.4:p.Tyr251Asp
|
|
ENST00000395331.3:c.829T>G
|
ENSP00000378740.3:p.Tyr277Asp
|
|
ENST00000395332.7:c.829T>G
|
ENSP00000378741.3:p.Tyr277Asp
|
|
ENST00000450043.2:c.142T>G
|
ENSP00000396527.2:p.Tyr48Asp
|
|
ENST00000493708.5:n.210T>G
|
|
|
NM_000048.3:c.829T>G
|
NP_000039.2:p.Tyr277Asp
|
|
NM_001024943.1:c.829T>G
|
NP_001020114.1:p.Tyr277Asp
|
|
NM_001024944.1:c.829T>G
|
NP_001020115.1:p.Tyr277Asp
|
|
NM_001024946.1:c.751T>G
|
NP_001020117.1:p.Tyr251Asp
|
|
NM_000048.4:c.829T>G
MANE Select
|
NP_000039.2:p.Tyr277Asp
|
|
NM_001024943.2:c.829T>G
|
NP_001020114.1:p.Tyr277Asp
|
|
NM_001024944.2:c.829T>G
|
NP_001020115.1:p.Tyr277Asp
|
|
NM_001024946.2:c.751T>G
|
NP_001020117.1:p.Tyr251Asp
|
|