ENST00000471476.2:c.*1413G>T
|
ENSP00000497663.1:n.*1413G>T
|
|
ENST00000647645.1:c.1771G>T
|
ENSP00000497450.1:p.Asp591Tyr
|
|
ENST00000647730.1:c.*1524G>T
|
ENSP00000497781.1:n.*1524G>T
|
|
ENST00000647788.1:c.*978G>T
|
ENSP00000497769.1:n.*978G>T
|
|
ENST00000648271.1:c.*2300G>T
|
ENSP00000497795.1:n.*2300G>T
|
|
ENST00000648807.1:c.1681G>T
|
ENSP00000497472.1:p.Asp561Tyr
|
|
ENST00000648960.1:c.1351G>T
|
ENSP00000497091.1:p.Asp451Tyr
|
|
ENST00000649067.1:c.*837G>T
|
ENSP00000497052.1:n.*837G>T
|
|
ENST00000649689.2:c.1834G>T
MANE Select
|
ENSP00000497569.1:p.Asp612Tyr
|
|
ENST00000361951.4:c.1834G>T
|
ENSP00000355086.4:p.Asp612Tyr
|
|
ENST00000471476.1:n.656G>T
|
|
|
NM_018122.4:c.1834G>T
|
NP_060592.2:p.Asp612Tyr
|
|
XM_006711427.2:c.1681G>T
|
XP_006711490.1:p.Asp561Tyr
|
|
NM_001365212.1:c.1681G>T
|
NP_001352141.1:p.Asp561Tyr
|
|
NM_018122.5:c.1834G>T
MANE Select
|
NP_060592.2:p.Asp612Tyr
|
|