ENST00000542672.7:c.2138C>T
|
ENSP00000443495.1:p.Thr713Met
|
|
ENST00000461367.2:n.434C>T
|
|
|
ENST00000492634.7:n.2068C>T
|
|
|
ENST00000682015.1:c.2045C>T
|
ENSP00000506961.1:p.Thr682Met
|
|
ENST00000682692.1:n.3233C>T
|
|
|
ENST00000682966.1:n.7779C>T
|
|
|
ENST00000683111.1:c.*1424C>T
|
ENSP00000507913.1:n.*1424C>T
|
|
ENST00000683322.1:n.3490C>T
|
|
|
ENST00000683805.1:n.929C>T
|
|
|
ENST00000684050.1:n.4776C>T
|
|
|
ENST00000684122.1:n.285C>T
|
|
|
ENST00000684286.1:n.3693C>T
|
|
|
ENST00000684502.1:n.3435C>T
|
|
|
ENST00000684763.1:n.753C>T
|
|
|
ENST00000366578.6:c.2138C>T
MANE Select
|
ENSP00000355537.4:p.Thr713Met
|
|
ENST00000492634.6:n.2068C>T
|
|
|
ENST00000542672.6:c.2138C>T
|
ENSP00000443495.1:p.Thr713Met
|
|
ENST00000651091.1:c.1828C>T
|
ENSP00000498677.1:n.1828C>T
|
|
ENST00000651275.1:c.2030C>T
|
ENSP00000498926.1:p.Thr677Met
|
|
ENST00000651781.1:c.1218C>T
|
|
|
ENST00000651786.1:c.*1510C>T
|
ENSP00000498364.1:n.*1510C>T
|
|
ENST00000652096.1:c.*1543C>T
|
ENSP00000498896.1:n.*1543C>T
|
|
ENST00000366578.5:c.2138C>T
|
ENSP00000355537.4:p.Thr713Met
|
|
ENST00000461367.1:n.347C>T
|
|
|
ENST00000542672.5:c.2138C>T
|
ENSP00000443495.1:p.Thr713Met
|
|
ENST00000546208.5:c.1514C>T
|
ENSP00000438384.2:p.Thr505Met
|
|
NM_001103.3:c.2138C>T
|
NP_001094.1:p.Thr713Met
|
|
NM_001278343.1:c.2138C>T
|
NP_001265272.1:p.Thr713Met
|
|
NM_001278344.1:c.1514C>T
|
NP_001265273.1:p.Thr505Met
|
|
NM_001278343.2:c.2138C>T
|
NP_001265272.1:p.Thr713Met
|
|
NM_001103.4:c.2138C>T
MANE Select
|
NP_001094.1:p.Thr713Met
|
|
NM_001278344.2:c.1514C>T
|
NP_001265273.1:p.Thr505Met
|
|