|
NM_003680.4:c.620G>A
MANE Select
|
NP_003671.1:p.Arg207Gln
|
|
ENST00000373477.9:c.620G>A
MANE Select
|
ENSP00000362576.4:p.Arg207Gln
|
|
NM_003680.3:c.620G>A , LRG_273t1:c.620G>A
|
NP_003671.1:p.Arg207Gln
|
|
ENST00000373477.8:c.620G>A
|
ENSP00000362576.4:p.Arg207Gln
|
|
ENST00000466052.1:n.528G>A
|
|
|
ENST00000470377.1:n.209G>A
|
|
|
ENST00000481895.5:n.740G>A
|
|
|
ENST00000481895.6:c.*454-3845G>A
|
ENSP00000502016.1:n.*454-3845G>A
|
|
ENST00000616261.1:c.620G>A
|
ENSP00000484192.1:p.Arg207Gln
|
|
ENST00000616261.2:c.667G>A
|
ENSP00000484192.2:p.Gly223Arg
|
|
ENST00000674629.1:c.*168G>A
|
ENSP00000502470.1:n.*168G>A
|
|
ENST00000674654.1:c.*88G>A
|
ENSP00000501729.1:n.*88G>A
|
|
ENST00000675785.1:c.473G>A
|
ENSP00000502019.1:p.Arg158Gln
|
|
ENST00000675785.2:c.473G>A
|
ENSP00000502019.1:p.Arg158Gln
|
|
ENST00000676297.1:c.*302G>A
|
ENSP00000501596.1:n.*302G>A
|
|
XM_011542347.1:c.-11G>A
|
XP_011540649.1:n.-11G>A
|
|
XM_011542347.2:c.-11G>A
|
XP_011540649.1:n.-11G>A
|
|
XM_011542348.1:c.-11G>A
|
XP_011540650.1:n.-11G>A
|
|
XM_017002651.2:c.-11G>A
|
XP_016858140.1:n.-11G>A
|