ENST00000542672.7:c.2060A>T
|
ENSP00000443495.1:p.Asn687Ile
|
|
ENST00000461367.2:n.356A>T
|
|
|
ENST00000492634.7:n.1990A>T
|
|
|
ENST00000682015.1:c.1967A>T
|
ENSP00000506961.1:p.Asn656Ile
|
|
ENST00000682692.1:n.3155A>T
|
|
|
ENST00000682966.1:n.7701A>T
|
|
|
ENST00000683111.1:c.*1346A>T
|
ENSP00000507913.1:n.*1346A>T
|
|
ENST00000683322.1:n.3412A>T
|
|
|
ENST00000683805.1:n.851A>T
|
|
|
ENST00000684050.1:n.4698A>T
|
|
|
ENST00000684122.1:n.207A>T
|
|
|
ENST00000684286.1:n.3615A>T
|
|
|
ENST00000684502.1:n.3357A>T
|
|
|
ENST00000684763.1:n.675A>T
|
|
|
ENST00000366578.6:c.2060A>T
MANE Select
|
ENSP00000355537.4:p.Asn687Ile
|
|
ENST00000492634.6:n.1990A>T
|
|
|
ENST00000542672.6:c.2060A>T
|
ENSP00000443495.1:p.Asn687Ile
|
|
ENST00000651091.1:c.1750A>T
|
ENSP00000498677.1:n.1750A>T
|
|
ENST00000651275.1:c.1952A>T
|
ENSP00000498926.1:p.Asn651Ile
|
|
ENST00000651781.1:c.1140A>T
|
|
|
ENST00000651786.1:c.*1432A>T
|
ENSP00000498364.1:n.*1432A>T
|
|
ENST00000652096.1:c.*1465A>T
|
ENSP00000498896.1:n.*1465A>T
|
|
ENST00000366578.5:c.2060A>T
|
ENSP00000355537.4:p.Asn687Ile
|
|
ENST00000461367.1:n.269A>T
|
|
|
ENST00000542672.5:c.2060A>T
|
ENSP00000443495.1:p.Asn687Ile
|
|
ENST00000546208.5:c.1436A>T
|
ENSP00000438384.2:p.Asn479Ile
|
|
NM_001103.3:c.2060A>T
|
NP_001094.1:p.Asn687Ile
|
|
NM_001278343.1:c.2060A>T
|
NP_001265272.1:p.Asn687Ile
|
|
NM_001278344.1:c.1436A>T
|
NP_001265273.1:p.Asn479Ile
|
|
NM_001278343.2:c.2060A>T
|
NP_001265272.1:p.Asn687Ile
|
|
NM_001103.4:c.2060A>T
MANE Select
|
NP_001094.1:p.Asn687Ile
|
|
NM_001278344.2:c.1436A>T
|
NP_001265273.1:p.Asn479Ile
|
|