ENST00000542672.7:c.2666A>C
|
ENSP00000443495.1:p.Tyr889Ser
|
|
ENST00000461367.2:n.962A>C
|
|
|
ENST00000492634.7:n.2596A>C
|
|
|
ENST00000682015.1:c.2573A>C
|
ENSP00000506961.1:p.Tyr858Ser
|
|
ENST00000682490.1:n.584A>C
|
|
|
ENST00000682692.1:n.3761A>C
|
|
|
ENST00000682966.1:n.8307A>C
|
|
|
ENST00000683111.1:c.*1952A>C
|
ENSP00000507913.1:n.*1952A>C
|
|
ENST00000683322.1:n.4018A>C
|
|
|
ENST00000683805.1:n.1457A>C
|
|
|
ENST00000684050.1:n.5304A>C
|
|
|
ENST00000684122.1:n.2100A>C
|
|
|
ENST00000684286.1:n.4221A>C
|
|
|
ENST00000684502.1:n.3963A>C
|
|
|
ENST00000684763.1:n.1281A>C
|
|
|
ENST00000366578.6:c.2666A>C
MANE Select
|
ENSP00000355537.4:p.Tyr889Ser
|
|
ENST00000492634.6:n.2596A>C
|
|
|
ENST00000542672.6:c.2666A>C
|
ENSP00000443495.1:p.Tyr889Ser
|
|
ENST00000651275.1:c.2558A>C
|
ENSP00000498926.1:p.Tyr853Ser
|
|
ENST00000651781.1:c.1746A>C
|
|
|
ENST00000651786.1:c.*2038A>C
|
ENSP00000498364.1:n.*2038A>C
|
|
ENST00000652096.1:c.*2071A>C
|
ENSP00000498896.1:n.*2071A>C
|
|
ENST00000366578.5:c.2666A>C
|
ENSP00000355537.4:p.Tyr889Ser
|
|
ENST00000542672.5:c.2666A>C
|
ENSP00000443495.1:p.Tyr889Ser
|
|
ENST00000546208.5:c.2042A>C
|
ENSP00000438384.2:p.Tyr681Ser
|
|
NM_001103.3:c.2666A>C
|
NP_001094.1:p.Tyr889Ser
|
|
NM_001278343.1:c.2666A>C
|
NP_001265272.1:p.Tyr889Ser
|
|
NM_001278344.1:c.2042A>C
|
NP_001265273.1:p.Tyr681Ser
|
|
NM_001278343.2:c.2666A>C
|
NP_001265272.1:p.Tyr889Ser
|
|
NM_001103.4:c.2666A>C
MANE Select
|
NP_001094.1:p.Tyr889Ser
|
|
NM_001278344.2:c.2042A>C
|
NP_001265273.1:p.Tyr681Ser
|
|