ENST00000542672.7:c.1963A>T
|
ENSP00000443495.1:p.Asn655Tyr
|
|
ENST00000461367.2:n.259A>T
|
|
|
ENST00000492634.7:n.1893A>T
|
|
|
ENST00000682015.1:c.1870A>T
|
ENSP00000506961.1:p.Asn624Tyr
|
|
ENST00000682692.1:n.3058A>T
|
|
|
ENST00000682966.1:n.7604A>T
|
|
|
ENST00000683111.1:c.*1249A>T
|
ENSP00000507913.1:n.*1249A>T
|
|
ENST00000683322.1:n.3315A>T
|
|
|
ENST00000684050.1:n.4601A>T
|
|
|
ENST00000684286.1:n.3518A>T
|
|
|
ENST00000684502.1:n.3260A>T
|
|
|
ENST00000684763.1:n.578A>T
|
|
|
ENST00000366578.6:c.1963A>T
MANE Select
|
ENSP00000355537.4:p.Asn655Tyr
|
|
ENST00000492634.6:n.1893A>T
|
|
|
ENST00000542672.6:c.1963A>T
|
ENSP00000443495.1:p.Asn655Tyr
|
|
ENST00000651091.1:c.1653A>T
|
ENSP00000498677.1:n.1653A>T
|
|
ENST00000651275.1:c.1855A>T
|
ENSP00000498926.1:p.Asn619Tyr
|
|
ENST00000651781.1:c.1043A>T
|
|
|
ENST00000651786.1:c.*1335A>T
|
ENSP00000498364.1:n.*1335A>T
|
|
ENST00000652096.1:c.*1368A>T
|
ENSP00000498896.1:n.*1368A>T
|
|
ENST00000366578.5:c.1963A>T
|
ENSP00000355537.4:p.Asn655Tyr
|
|
ENST00000461367.1:n.172A>T
|
|
|
ENST00000542672.5:c.1963A>T
|
ENSP00000443495.1:p.Asn655Tyr
|
|
ENST00000546208.5:c.1339A>T
|
ENSP00000438384.2:p.Asn447Tyr
|
|
NM_001103.3:c.1963A>T
|
NP_001094.1:p.Asn655Tyr
|
|
NM_001278343.1:c.1963A>T
|
NP_001265272.1:p.Asn655Tyr
|
|
NM_001278344.1:c.1339A>T
|
NP_001265273.1:p.Asn447Tyr
|
|
NM_001278343.2:c.1963A>T
|
NP_001265272.1:p.Asn655Tyr
|
|
NM_001103.4:c.1963A>T
MANE Select
|
NP_001094.1:p.Asn655Tyr
|
|
NM_001278344.2:c.1339A>T
|
NP_001265273.1:p.Asn447Tyr
|
|