ENST00000326003.7:c.748C>A
MANE Select
|
ENSP00000314151.1:p.Arg250=
|
|
ENST00000326003.6:c.748C>A
|
ENSP00000314151.1:p.Arg250=
|
|
ENST00000360617.7:c.1190C>A
|
ENSP00000353829.2:n.1190C>A
|
|
ENST00000422986.6:c.*404C>A
|
ENSP00000393628.2:n.*404C>A
|
|
ENST00000595392.5:c.*249C>A
|
ENSP00000468912.1:n.*249C>A
|
|
ENST00000595952.5:c.619C>A
|
ENSP00000471155.1:p.Arg207=
|
|
ENST00000596333.1:n.926C>A
|
|
|
ENST00000598145.1:c.750C>A
|
|
|
ENST00000601349.5:n.2027C>A
|
|
|
ENST00000601812.1:n.1180C>A
|
|
|
ENST00000617027.4:c.625C>A
|
ENSP00000483513.1:p.Arg209=
|
|
NM_001030047.1:c.*473C>A
|
NP_001025218.1:n.*473C>A
|
|
NM_001030048.1:c.619C>A
|
NP_001025219.1:p.Arg207=
|
|
NM_001648.2:c.748C>A
MANE Select
|
NP_001639.1:p.Arg250=
|
|
XM_011526923.1:c.766C>A
|
XP_011525225.1:p.Arg256=
|
|
XR_935817.1:n.1324+835C>A
|
|
|