ENST00000471476.2:c.*1376A>C
|
ENSP00000497663.1:n.*1376A>C
|
|
ENST00000647645.1:c.1734A>C
|
ENSP00000497450.1:p.Arg578Ser
|
|
ENST00000647730.1:c.*1487A>C
|
ENSP00000497781.1:n.*1487A>C
|
|
ENST00000647788.1:c.*941A>C
|
ENSP00000497769.1:n.*941A>C
|
|
ENST00000648271.1:c.*2263A>C
|
ENSP00000497795.1:n.*2263A>C
|
|
ENST00000648807.1:c.1644A>C
|
ENSP00000497472.1:p.Arg548Ser
|
|
ENST00000648960.1:c.1314A>C
|
ENSP00000497091.1:p.Arg438Ser
|
|
ENST00000649067.1:c.*800A>C
|
ENSP00000497052.1:n.*800A>C
|
|
ENST00000649689.2:c.1797A>C
MANE Select
|
ENSP00000497569.1:p.Arg599Ser
|
|
ENST00000361951.4:c.1797A>C
|
ENSP00000355086.4:p.Arg599Ser
|
|
ENST00000471476.1:n.619A>C
|
|
|
NM_018122.4:c.1797A>C
|
NP_060592.2:p.Arg599Ser
|
|
XM_006711427.2:c.1644A>C
|
XP_006711490.1:p.Arg548Ser
|
|
NM_001365212.1:c.1644A>C
|
NP_001352141.1:p.Arg548Ser
|
|
NM_018122.5:c.1797A>C
MANE Select
|
NP_060592.2:p.Arg599Ser
|
|