ENST00000471476.2:c.*1378A>C
|
ENSP00000497663.1:n.*1378A>C
|
|
ENST00000647645.1:c.1736A>C
|
ENSP00000497450.1:p.Asp579Ala
|
|
ENST00000647730.1:c.*1489A>C
|
ENSP00000497781.1:n.*1489A>C
|
|
ENST00000647788.1:c.*943A>C
|
ENSP00000497769.1:n.*943A>C
|
|
ENST00000648271.1:c.*2265A>C
|
ENSP00000497795.1:n.*2265A>C
|
|
ENST00000648807.1:c.1646A>C
|
ENSP00000497472.1:p.Asp549Ala
|
|
ENST00000648960.1:c.1316A>C
|
ENSP00000497091.1:p.Asp439Ala
|
|
ENST00000649067.1:c.*802A>C
|
ENSP00000497052.1:n.*802A>C
|
|
ENST00000649689.2:c.1799A>C
MANE Select
|
ENSP00000497569.1:p.Asp600Ala
|
|
ENST00000361951.4:c.1799A>C
|
ENSP00000355086.4:p.Asp600Ala
|
|
ENST00000471476.1:n.621A>C
|
|
|
NM_018122.4:c.1799A>C
|
NP_060592.2:p.Asp600Ala
|
|
XM_006711427.2:c.1646A>C
|
XP_006711490.1:p.Asp549Ala
|
|
NM_001365212.1:c.1646A>C
|
NP_001352141.1:p.Asp549Ala
|
|
NM_018122.5:c.1799A>C
MANE Select
|
NP_060592.2:p.Asp600Ala
|
|