ENST00000682422.1:n.887T>C
|
|
|
ENST00000682545.1:c.*312T>C
|
ENSP00000508402.1:n.*312T>C
|
|
ENST00000682887.1:c.1707T>C
|
ENSP00000506946.1:n.1707T>C
|
|
ENST00000683302.1:c.1237T>C
|
ENSP00000507885.1:p.Cys413Arg
|
|
ENST00000683557.1:c.*138T>C
|
ENSP00000508029.1:n.*138T>C
|
|
ENST00000367282.6:c.1306T>C
MANE Select
|
ENSP00000356251.4:p.Cys436Arg
|
|
ENST00000367282.5:c.1306T>C
|
ENSP00000356251.4:p.Cys436Arg
|
|
NM_004767.3:c.1306T>C
|
NP_004758.3:p.Cys436Arg
|
|
XM_011510158.1:c.745T>C
|
XP_011508460.1:p.Cys249Arg
|
|
NM_004767.4:c.1306T>C
|
NP_004758.3:p.Cys436Arg
|
|
XM_011510158.2:c.745T>C
|
XP_011508460.1:p.Cys249Arg
|
|
NM_004767.5:c.1306T>C
MANE Select
|
NP_004758.3:p.Cys436Arg
|
|