ENST00000304895.9:c.1938A>G
MANE Select
|
ENSP00000302728.4:p.Glu646=
|
|
ENST00000304895.8:c.1938A>G
|
ENSP00000302728.4:p.Glu646=
|
|
ENST00000421103.5:c.1500A>G
|
ENSP00000391390.1:p.Glu500=
|
|
ENST00000430730.5:c.*1205A>G
|
ENSP00000411859.1:n.*1205A>G
|
|
ENST00000447929.5:c.*1318A>G
|
ENSP00000411262.1:n.*1318A>G
|
|
ENST00000466883.5:n.2328A>G
|
|
|
NM_000181.3:c.1938A>G
|
NP_000172.2:p.Glu646=
|
|
NM_001284290.1:c.1500A>G
|
NP_001271219.1:p.Glu500=
|
|
NM_001293104.1:c.1368A>G
|
NP_001280033.1:p.Glu456=
|
|
NM_001293105.1:c.1281A>G
|
NP_001280034.1:p.Glu427=
|
|
NR_120531.1:n.1984A>G
|
|
|
XM_005250297.3:c.1785A>G
|
XP_005250354.1:p.Glu595=
|
|
XM_011516113.1:c.1437A>G
|
XP_011514415.1:p.Glu479=
|
|
XM_011516114.1:c.1266A>G
|
XP_011514416.1:p.Glu422=
|
|
XM_005250297.4:c.1785A>G
|
XP_005250354.1:p.Glu595=
|
|
XM_011516114.2:c.1266A>G
|
XP_011514416.1:p.Glu422=
|
|
XM_017012091.1:c.1284A>G
|
XP_016867580.1:p.Glu428=
|
|
XM_017012092.1:c.1215A>G
|
XP_016867581.1:p.Glu405=
|
|
XM_017012093.2:c.1113A>G
|
XP_016867582.1:p.Glu371=
|
|
XR_001744658.2:n.1745A>G
|
|
|
XR_001744659.2:n.1858A>G
|
|
|
XR_001744660.2:n.1790A>G
|
|
|
XR_001744661.2:n.1705A>G
|
|
|
XR_927461.3:n.1943A>G
|
|
|
NM_000181.4:c.1938A>G
MANE Select
|
NP_000172.2:p.Glu646=
|
|
NM_001284290.2:c.1500A>G
|
NP_001271219.1:p.Glu500=
|
|
NM_001293104.2:c.1368A>G
|
NP_001280033.1:p.Glu456=
|
|
NM_001293105.2:c.1281A>G
|
NP_001280034.1:p.Glu427=
|
|
NR_120531.2:n.1883A>G
|
|
|