ENST00000304895.9:c.1929A>T
MANE Select
|
ENSP00000302728.4:p.Gln643His
|
|
ENST00000304895.8:c.1929A>T
|
ENSP00000302728.4:p.Gln643His
|
|
ENST00000421103.5:c.1491A>T
|
ENSP00000391390.1:p.Gln497His
|
|
ENST00000430730.5:c.*1196A>T
|
ENSP00000411859.1:n.*1196A>T
|
|
ENST00000447929.5:c.*1309A>T
|
ENSP00000411262.1:n.*1309A>T
|
|
ENST00000466883.5:n.2319A>T
|
|
|
NM_000181.3:c.1929A>T
|
NP_000172.2:p.Gln643His
|
|
NM_001284290.1:c.1491A>T
|
NP_001271219.1:p.Gln497His
|
|
NM_001293104.1:c.1359A>T
|
NP_001280033.1:p.Gln453His
|
|
NM_001293105.1:c.1272A>T
|
NP_001280034.1:p.Gln424His
|
|
NR_120531.1:n.1975A>T
|
|
|
XM_005250297.3:c.1776A>T
|
XP_005250354.1:p.Gln592His
|
|
XM_011516113.1:c.1428A>T
|
XP_011514415.1:p.Gln476His
|
|
XM_011516114.1:c.1257A>T
|
XP_011514416.1:p.Gln419His
|
|
XM_005250297.4:c.1776A>T
|
XP_005250354.1:p.Gln592His
|
|
XM_011516114.2:c.1257A>T
|
XP_011514416.1:p.Gln419His
|
|
XM_017012091.1:c.1275A>T
|
XP_016867580.1:p.Gln425His
|
|
XM_017012092.1:c.1206A>T
|
XP_016867581.1:p.Gln402His
|
|
XM_017012093.2:c.1104A>T
|
XP_016867582.1:p.Gln368His
|
|
XR_001744658.2:n.1736A>T
|
|
|
XR_001744659.2:n.1849A>T
|
|
|
XR_001744660.2:n.1781A>T
|
|
|
XR_001744661.2:n.1696A>T
|
|
|
XR_927461.3:n.1934A>T
|
|
|
NM_000181.4:c.1929A>T
MANE Select
|
NP_000172.2:p.Gln643His
|
|
NM_001284290.2:c.1491A>T
|
NP_001271219.1:p.Gln497His
|
|
NM_001293104.2:c.1359A>T
|
NP_001280033.1:p.Gln453His
|
|
NM_001293105.2:c.1272A>T
|
NP_001280034.1:p.Gln424His
|
|
NR_120531.2:n.1874A>T
|
|
|