ENST00000304895.9:c.1869A>G
MANE Select
|
ENSP00000302728.4:p.Arg623=
|
|
ENST00000304895.8:c.1869A>G
|
ENSP00000302728.4:p.Arg623=
|
|
ENST00000421103.5:c.1431A>G
|
ENSP00000391390.1:p.Arg477=
|
|
ENST00000430730.5:c.*1136A>G
|
ENSP00000411859.1:n.*1136A>G
|
|
ENST00000447929.5:c.*1249A>G
|
ENSP00000411262.1:n.*1249A>G
|
|
ENST00000466883.5:n.2259A>G
|
|
|
NM_000181.3:c.1869A>G
|
NP_000172.2:p.Arg623=
|
|
NM_001284290.1:c.1431A>G
|
NP_001271219.1:p.Arg477=
|
|
NM_001293104.1:c.1299A>G
|
NP_001280033.1:p.Arg433=
|
|
NM_001293105.1:c.1212A>G
|
NP_001280034.1:p.Arg404=
|
|
NR_120531.1:n.1915A>G
|
|
|
XM_005250297.3:c.1716A>G
|
XP_005250354.1:p.Arg572=
|
|
XM_011516113.1:c.1368A>G
|
XP_011514415.1:p.Arg456=
|
|
XM_011516114.1:c.1197A>G
|
XP_011514416.1:p.Arg399=
|
|
XM_005250297.4:c.1716A>G
|
XP_005250354.1:p.Arg572=
|
|
XM_011516114.2:c.1197A>G
|
XP_011514416.1:p.Arg399=
|
|
XM_017012091.1:c.1215A>G
|
XP_016867580.1:p.Arg405=
|
|
XM_017012092.1:c.1146A>G
|
XP_016867581.1:p.Arg382=
|
|
XM_017012093.2:c.1044A>G
|
XP_016867582.1:p.Arg348=
|
|
XR_001744658.2:n.1676A>G
|
|
|
XR_001744659.2:n.1789A>G
|
|
|
XR_001744660.2:n.1721A>G
|
|
|
XR_001744661.2:n.1636A>G
|
|
|
XR_927461.3:n.1874A>G
|
|
|
NM_000181.4:c.1869A>G
MANE Select
|
NP_000172.2:p.Arg623=
|
|
NM_001284290.2:c.1431A>G
|
NP_001271219.1:p.Arg477=
|
|
NM_001293104.2:c.1299A>G
|
NP_001280033.1:p.Arg433=
|
|
NM_001293105.2:c.1212A>G
|
NP_001280034.1:p.Arg404=
|
|
NR_120531.2:n.1814A>G
|
|
|