ENST00000309383.6:c.2112A>C
MANE Select
|
ENSP00000310649.1:p.Arg704=
|
|
ENST00000309383.5:c.2112A>C
|
ENSP00000310649.1:p.Arg704=
|
|
ENST00000326848.7:c.1197A>C
|
ENSP00000320853.7:p.Arg399=
|
|
ENST00000590333.5:c.2160A>C
|
ENSP00000468190.1:p.Arg720=
|
|
NM_032430.1:c.2112A>C
|
NP_115806.1:p.Arg704=
|
|
XM_005259327.2:c.1842A>C
|
XP_005259384.1:p.Arg614=
|
|
XM_011527395.1:c.1869A>C
|
XP_011525697.1:p.Arg623=
|
|
XR_430213.2:n.2095A>C
|
|
|
XM_005259327.3:c.1842A>C
|
XP_005259384.1:p.Arg614=
|
|
XM_011527395.2:c.1584A>C
|
XP_011525697.2:p.Arg528=
|
|
XM_024451739.1:c.1887A>C
|
XP_024307507.1:p.Arg629=
|
|
XR_430213.4:n.2393A>C
|
|
|
NM_032430.2:c.2112A>C
MANE Select
|
NP_115806.1:p.Arg704=
|
|