ENST00000471476.2:c.*1336A>C
|
ENSP00000497663.1:n.*1336A>C
|
|
ENST00000647645.1:c.1694A>C
|
ENSP00000497450.1:p.Asp565Ala
|
|
ENST00000647730.1:c.*1447A>C
|
ENSP00000497781.1:n.*1447A>C
|
|
ENST00000647788.1:c.*901A>C
|
ENSP00000497769.1:n.*901A>C
|
|
ENST00000648271.1:c.*2223A>C
|
ENSP00000497795.1:n.*2223A>C
|
|
ENST00000648807.1:c.1604A>C
|
ENSP00000497472.1:p.Asp535Ala
|
|
ENST00000648960.1:c.1274A>C
|
ENSP00000497091.1:p.Asp425Ala
|
|
ENST00000649067.1:c.*760A>C
|
ENSP00000497052.1:n.*760A>C
|
|
ENST00000649689.2:c.1757A>C
MANE Select
|
ENSP00000497569.1:p.Asp586Ala
|
|
ENST00000361951.4:c.1757A>C
|
ENSP00000355086.4:p.Asp586Ala
|
|
ENST00000471476.1:n.579A>C
|
|
|
NM_018122.4:c.1757A>C
|
NP_060592.2:p.Asp586Ala
|
|
XM_006711427.2:c.1604A>C
|
XP_006711490.1:p.Asp535Ala
|
|
NM_001365212.1:c.1604A>C
|
NP_001352141.1:p.Asp535Ala
|
|
NM_018122.5:c.1757A>C
MANE Select
|
NP_060592.2:p.Asp586Ala
|
|