ENST00000471476.2:c.*1388C>T
|
ENSP00000497663.1:n.*1388C>T
|
|
ENST00000647645.1:c.1746C>T
|
ENSP00000497450.1:p.Ala582=
|
|
ENST00000647730.1:c.*1499C>T
|
ENSP00000497781.1:n.*1499C>T
|
|
ENST00000647788.1:c.*953C>T
|
ENSP00000497769.1:n.*953C>T
|
|
ENST00000648271.1:c.*2275C>T
|
ENSP00000497795.1:n.*2275C>T
|
|
ENST00000648807.1:c.1656C>T
|
ENSP00000497472.1:p.Ala552=
|
|
ENST00000648960.1:c.1326C>T
|
ENSP00000497091.1:p.Ala442=
|
|
ENST00000649067.1:c.*812C>T
|
ENSP00000497052.1:n.*812C>T
|
|
ENST00000649689.2:c.1809C>T
MANE Select
|
ENSP00000497569.1:p.Ala603=
|
|
ENST00000361951.4:c.1809C>T
|
ENSP00000355086.4:p.Ala603=
|
|
ENST00000471476.1:n.631C>T
|
|
|
NM_018122.4:c.1809C>T
|
NP_060592.2:p.Ala603=
|
|
XM_006711427.2:c.1656C>T
|
XP_006711490.1:p.Ala552=
|
|
NM_001365212.1:c.1656C>T
|
NP_001352141.1:p.Ala552=
|
|
NM_018122.5:c.1809C>T
MANE Select
|
NP_060592.2:p.Ala603=
|
|