ENST00000542672.7:c.2120T>C
|
ENSP00000443495.1:p.Val707Ala
|
|
ENST00000461367.2:n.416T>C
|
|
|
ENST00000492634.7:n.2050T>C
|
|
|
ENST00000682015.1:c.2027T>C
|
ENSP00000506961.1:p.Val676Ala
|
|
ENST00000682692.1:n.3215T>C
|
|
|
ENST00000682966.1:n.7761T>C
|
|
|
ENST00000683111.1:c.*1406T>C
|
ENSP00000507913.1:n.*1406T>C
|
|
ENST00000683322.1:n.3472T>C
|
|
|
ENST00000683805.1:n.911T>C
|
|
|
ENST00000684050.1:n.4758T>C
|
|
|
ENST00000684122.1:n.267T>C
|
|
|
ENST00000684286.1:n.3675T>C
|
|
|
ENST00000684502.1:n.3417T>C
|
|
|
ENST00000684763.1:n.735T>C
|
|
|
ENST00000366578.6:c.2120T>C
MANE Select
|
ENSP00000355537.4:p.Val707Ala
|
|
ENST00000492634.6:n.2050T>C
|
|
|
ENST00000542672.6:c.2120T>C
|
ENSP00000443495.1:p.Val707Ala
|
|
ENST00000651091.1:c.1810T>C
|
ENSP00000498677.1:n.1810T>C
|
|
ENST00000651275.1:c.2012T>C
|
ENSP00000498926.1:p.Val671Ala
|
|
ENST00000651781.1:c.1200T>C
|
|
|
ENST00000651786.1:c.*1492T>C
|
ENSP00000498364.1:n.*1492T>C
|
|
ENST00000652096.1:c.*1525T>C
|
ENSP00000498896.1:n.*1525T>C
|
|
ENST00000366578.5:c.2120T>C
|
ENSP00000355537.4:p.Val707Ala
|
|
ENST00000461367.1:n.329T>C
|
|
|
ENST00000542672.5:c.2120T>C
|
ENSP00000443495.1:p.Val707Ala
|
|
ENST00000546208.5:c.1496T>C
|
ENSP00000438384.2:p.Val499Ala
|
|
NM_001103.3:c.2120T>C
|
NP_001094.1:p.Val707Ala
|
|
NM_001278343.1:c.2120T>C
|
NP_001265272.1:p.Val707Ala
|
|
NM_001278344.1:c.1496T>C
|
NP_001265273.1:p.Val499Ala
|
|
NM_001278343.2:c.2120T>C
|
NP_001265272.1:p.Val707Ala
|
|
NM_001103.4:c.2120T>C
MANE Select
|
NP_001094.1:p.Val707Ala
|
|
NM_001278344.2:c.1496T>C
|
NP_001265273.1:p.Val499Ala
|
|