ENST00000703783.1:n.664T>C
|
|
|
ENST00000703785.1:n.745T>C
|
|
|
ENST00000262464.9:c.3880T>C
MANE Select
|
ENSP00000262464.4:p.Cys1294Arg
|
|
ENST00000262464.8:c.3880T>C
|
ENSP00000262464.4:p.Cys1294Arg
|
|
ENST00000507835.5:c.430T>C
|
ENSP00000426839.1:p.Cys144Arg
|
|
ENST00000508053.5:c.3880T>C
|
ENSP00000424571.1:p.Cys1294Arg
|
|
ENST00000508989.5:c.3781T>C
|
ENSP00000425596.1:p.Cys1261Arg
|
|
ENST00000619499.4:c.3877T>C
|
ENSP00000482132.1:p.Cys1293Arg
|
|
NM_001999.3:c.3880T>C
|
NP_001990.2:p.Cys1294Arg
|
|
XM_017009228.2:c.3727T>C
|
XP_016864717.1:p.Cys1243Arg
|
|
NM_001999.4:c.3880T>C
MANE Select
|
NP_001990.2:p.Cys1294Arg
|
|