ENST00000326003.7:c.784T>C
MANE Select
|
ENSP00000314151.1:p.Ter262Arg
|
|
ENST00000326003.6:c.784T>C
|
ENSP00000314151.1:p.Ter262Arg
|
|
ENST00000360617.7:c.1226T>C
|
ENSP00000353829.2:n.1226T>C
|
|
ENST00000422986.6:c.*440T>C
|
ENSP00000393628.2:n.*440T>C
|
|
ENST00000595392.5:c.*285T>C
|
ENSP00000468912.1:n.*285T>C
|
|
ENST00000595952.5:c.655T>C
|
ENSP00000471155.1:p.Ter219Arg
|
|
ENST00000596333.1:n.962T>C
|
|
|
ENST00000598145.1:c.786T>C
|
|
|
ENST00000601349.5:n.2063T>C
|
|
|
ENST00000601812.1:n.1216T>C
|
|
|
ENST00000617027.4:c.661T>C
|
ENSP00000483513.1:p.Ter221Arg
|
|
NM_001030047.1:c.*509T>C
|
NP_001025218.1:n.*509T>C
|
|
NM_001030048.1:c.655T>C
|
NP_001025219.1:p.Ter219Arg
|
|
NM_001648.2:c.784T>C
MANE Select
|
NP_001639.1:p.Ter262Arg
|
|
XM_011526923.1:c.802T>C
|
XP_011525225.1:p.Ter268Arg
|
|
XR_935817.1:n.1324+871T>C
|
|
|