ENST00000396027.9:c.967A>C
MANE Select
|
ENSP00000379344.4:p.Arg323=
|
|
ENST00000282268.7:c.967A>C
|
ENSP00000282268.3:p.Arg323=
|
|
ENST00000338635.10:c.973A>C
|
ENSP00000342011.6:p.Arg325=
|
|
ENST00000396027.8:c.967A>C
|
ENSP00000379344.4:p.Arg323=
|
|
ENST00000511817.1:c.973A>C
|
ENSP00000421491.1:p.Arg325=
|
|
NM_003401.3:c.967A>C
|
NP_003392.1:p.Arg323=
|
|
NM_022406.2:c.973A>C
|
NP_071801.1:p.Arg325=
|
|
NM_022550.2:c.967A>C
|
NP_072044.1:p.Arg323=
|
|
XM_005248595.1:c.973A>C
|
XP_005248652.1:p.Arg325=
|
|
XM_011543626.1:c.973A>C
|
XP_011541928.1:p.Arg325=
|
|
XM_011543629.1:c.313A>C
|
XP_011541931.1:p.Arg105=
|
|
NM_001318012.1:c.973A>C
|
NP_001304941.1:p.Arg325=
|
|
NM_003401.4:c.967A>C
|
NP_003392.1:p.Arg323=
|
|
NM_022406.3:c.973A>C
|
NP_071801.1:p.Arg325=
|
|
NM_022550.3:c.967A>C
|
NP_072044.1:p.Arg323=
|
|
XM_017009827.2:c.894-17063A>C
|
XP_016865316.1:n.894-17063A>C
|
|
NM_001318012.2:c.973A>C
|
NP_001304941.1:p.Arg325=
|
|
NM_003401.5:c.967A>C
MANE Select
|
NP_003392.1:p.Arg323=
|
|
NM_022406.4:c.973A>C
|
NP_071801.1:p.Arg325=
|
|
NM_001318012.3:c.973A>C
|
NP_001304941.1:p.Arg325=
|
|
NM_022406.5:c.973A>C
|
NP_071801.1:p.Arg325=
|
|
NM_022550.4:c.967A>C
|
NP_072044.1:p.Arg323=
|
|