ENST00000542672.7:c.2656T>G
|
ENSP00000443495.1:p.Ser886Ala
|
|
ENST00000461367.2:n.952T>G
|
|
|
ENST00000492634.7:n.2586T>G
|
|
|
ENST00000682015.1:c.2563T>G
|
ENSP00000506961.1:p.Ser855Ala
|
|
ENST00000682490.1:n.574T>G
|
|
|
ENST00000682692.1:n.3751T>G
|
|
|
ENST00000682966.1:n.8297T>G
|
|
|
ENST00000683111.1:c.*1942T>G
|
ENSP00000507913.1:n.*1942T>G
|
|
ENST00000683322.1:n.4008T>G
|
|
|
ENST00000683805.1:n.1447T>G
|
|
|
ENST00000684050.1:n.5294T>G
|
|
|
ENST00000684122.1:n.2090T>G
|
|
|
ENST00000684286.1:n.4211T>G
|
|
|
ENST00000684502.1:n.3953T>G
|
|
|
ENST00000684763.1:n.1271T>G
|
|
|
ENST00000366578.6:c.2656T>G
MANE Select
|
ENSP00000355537.4:p.Ser886Ala
|
|
ENST00000492634.6:n.2586T>G
|
|
|
ENST00000542672.6:c.2656T>G
|
ENSP00000443495.1:p.Ser886Ala
|
|
ENST00000651091.1:c.2346T>G
|
ENSP00000498677.1:n.2346T>G
|
|
ENST00000651275.1:c.2548T>G
|
ENSP00000498926.1:p.Ser850Ala
|
|
ENST00000651781.1:c.1736T>G
|
|
|
ENST00000651786.1:c.*2028T>G
|
ENSP00000498364.1:n.*2028T>G
|
|
ENST00000652096.1:c.*2061T>G
|
ENSP00000498896.1:n.*2061T>G
|
|
ENST00000366578.5:c.2656T>G
|
ENSP00000355537.4:p.Ser886Ala
|
|
ENST00000542672.5:c.2656T>G
|
ENSP00000443495.1:p.Ser886Ala
|
|
ENST00000546208.5:c.2032T>G
|
ENSP00000438384.2:p.Ser678Ala
|
|
NM_001103.3:c.2656T>G
|
NP_001094.1:p.Ser886Ala
|
|
NM_001278343.1:c.2656T>G
|
NP_001265272.1:p.Ser886Ala
|
|
NM_001278344.1:c.2032T>G
|
NP_001265273.1:p.Ser678Ala
|
|
NM_001278343.2:c.2656T>G
|
NP_001265272.1:p.Ser886Ala
|
|
NM_001103.4:c.2656T>G
MANE Select
|
NP_001094.1:p.Ser886Ala
|
|
NM_001278344.2:c.2032T>G
|
NP_001265273.1:p.Ser678Ala
|
|