ENST00000354674.5:c.1778C>T
MANE Plus Clinical
|
ENSP00000346701.4:p.Ala593Val
|
|
ENST00000367255.10:c.25244C>T
MANE Select
|
ENSP00000356224.5:p.Ala8415Val
|
|
ENST00000423061.6:c.25100C>T
|
ENSP00000396024.1:p.Ala8367Val
|
|
ENST00000672154.1:c.646C>T
|
|
|
ENST00000672169.1:c.979C>T
|
|
|
ENST00000673173.1:c.891-1044C>T
|
|
|
ENST00000673451.1:c.1016C>T
|
ENSP00000500189.1:p.Ala339Val
|
|
ENST00000341594.9:c.24029C>T
|
ENSP00000341887.6:p.Ala8010Val
|
|
ENST00000347037.9:n.1992C>T
|
|
|
ENST00000354674.4:c.1778C>T
|
ENSP00000346701.4:p.Ala593Val
|
|
ENST00000367251.7:c.4079C>T
|
ENSP00000356220.3:p.Ala1360Val
|
|
ENST00000367255.9:c.25244C>T
|
ENSP00000356224.5:p.Ala8415Val
|
|
ENST00000367256.9:n.8936C>T
|
|
|
ENST00000367257.8:c.3182C>T
|
ENSP00000356226.4:p.Ala1061Val
|
|
ENST00000409694.6:n.8828C>T
|
|
|
ENST00000423061.5:c.25100C>T
|
ENSP00000396024.1:p.Ala8367Val
|
|
ENST00000460912.6:n.1858C>T
|
|
|
ENST00000478916.5:n.4266C>T
|
|
|
ENST00000536990.5:n.2081C>T
|
|
|
ENST00000539504.5:c.1709C>T
|
ENSP00000441052.1:p.Ala570Val
|
|
NM_033071.3:c.25100C>T
|
NP_149062.1:p.Ala8367Val
|
|
NM_182961.3:c.25244C>T
|
NP_892006.3:p.Ala8415Val
|
|
XM_006715407.1:c.25349C>T
|
XP_006715470.1:p.Ala8450Val
|
|
XM_006715408.1:c.25337C>T
|
XP_006715471.1:p.Ala8446Val
|
|
XM_006715409.1:c.25328C>T
|
XP_006715472.1:p.Ala8443Val
|
|
XM_006715410.1:c.25349C>T
|
XP_006715473.1:p.Ala8450Val
|
|
XM_006715411.1:c.25298C>T
|
XP_006715474.1:p.Ala8433Val
|
|
XM_006715412.1:c.25334C>T
|
XP_006715475.1:p.Ala8445Val
|
|
XM_006715413.1:c.25280C>T
|
XP_006715476.1:p.Ala8427Val
|
|
XM_006715414.1:c.25277C>T
|
XP_006715477.1:p.Ala8426Val
|
|
XM_006715415.1:c.25280C>T
|
XP_006715478.1:p.Ala8427Val
|
|
XM_006715416.1:c.25265C>T
|
XP_006715479.1:p.Ala8422Val
|
|
XM_006715417.1:c.25208C>T
|
XP_006715480.1:p.Ala8403Val
|
|
XM_006715420.1:c.25196C>T
|
XP_006715483.1:p.Ala8399Val
|
|
XM_006715421.1:c.25193C>T
|
XP_006715484.1:p.Ala8398Val
|
|
XM_006715422.1:c.25190C>T
|
XP_006715485.1:p.Ala8397Val
|
|
XM_006715423.1:c.25349C>T
|
XP_006715486.1:p.Ala8450Val
|
|
XM_006715424.1:c.25349C>T
|
XP_006715487.1:p.Ala8450Val
|
|
XM_006715425.1:c.25280C>T
|
XP_006715488.1:p.Ala8427Val
|
|
XM_011535641.1:c.25346C>T
|
XP_011533943.1:p.Ala8449Val
|
|
XM_011535642.1:c.25334C>T
|
XP_011533944.1:p.Ala8445Val
|
|
XM_011535643.1:c.25184C>T
|
XP_011533945.1:p.Ala8395Val
|
|
XM_011535644.1:c.23624C>T
|
XP_011533946.1:p.Ala7875Val
|
|
XM_011535645.1:c.23117C>T
|
XP_011533947.1:p.Ala7706Val
|
|
XM_011535647.1:c.18584C>T
|
XP_011533949.1:p.Ala6195Val
|
|
NM_001347701.1:c.1850C>T
|
NP_001334630.1:p.Ala617Val
|
|
NM_001347702.1:c.1778C>T
|
NP_001334631.1:p.Ala593Val
|
|
XM_006715408.2:c.25337C>T
|
XP_006715471.1:p.Ala8446Val
|
|
XM_006715410.2:c.25349C>T
|
XP_006715473.1:p.Ala8450Val
|
|
XM_006715412.2:c.25334C>T
|
XP_006715475.1:p.Ala8445Val
|
|
XM_006715413.2:c.25280C>T
|
XP_006715476.1:p.Ala8427Val
|
|
XM_006715415.2:c.25280C>T
|
XP_006715478.1:p.Ala8427Val
|
|
XM_006715416.2:c.25265C>T
|
XP_006715479.1:p.Ala8422Val
|
|
XM_006715417.2:c.25208C>T
|
XP_006715480.1:p.Ala8403Val
|
|
XM_006715420.2:c.25196C>T
|
XP_006715483.1:p.Ala8399Val
|
|
XM_006715421.2:c.25193C>T
|
XP_006715484.1:p.Ala8398Val
|
|
XM_006715423.2:c.25349C>T
|
XP_006715486.1:p.Ala8450Val
|
|
XM_006715424.2:c.25349C>T
|
XP_006715487.1:p.Ala8450Val
|
|
XM_006715425.2:c.25280C>T
|
XP_006715488.1:p.Ala8427Val
|
|
XM_011535641.2:c.25346C>T
|
XP_011533943.1:p.Ala8449Val
|
|
XM_011535642.2:c.25334C>T
|
XP_011533944.1:p.Ala8445Val
|
|
XM_011535645.2:c.23117C>T
|
XP_011533947.1:p.Ala7706Val
|
|
XM_017010608.1:c.25349C>T
|
XP_016866097.1:p.Ala8450Val
|
|
XM_017010609.1:c.25349C>T
|
XP_016866098.1:p.Ala8450Val
|
|
XM_017010610.1:c.25328C>T
|
XP_016866099.1:p.Ala8443Val
|
|
XM_017010611.2:c.25322C>T
|
XP_016866100.1:p.Ala8441Val
|
|
XM_017010612.1:c.25271C>T
|
XP_016866101.1:p.Ala8424Val
|
|
XM_017010613.1:c.25277C>T
|
XP_016866102.1:p.Ala8426Val
|
|
XM_017010614.1:c.25193C>T
|
XP_016866103.1:p.Ala8398Val
|
|
XM_017010615.1:c.25124C>T
|
XP_016866104.1:p.Ala8375Val
|
|
XM_017010616.1:c.25280C>T
|
XP_016866105.1:p.Ala8427Val
|
|
XM_017010617.1:c.25277C>T
|
XP_016866106.1:p.Ala8426Val
|
|
XM_017010618.1:c.25265C>T
|
XP_016866107.1:p.Ala8422Val
|
|
XM_017010619.1:c.23624C>T
|
XP_016866108.1:p.Ala7875Val
|
|
NM_182961.4:c.25244C>T
MANE Select
|
NP_892006.3:p.Ala8415Val
|
|
NM_001347701.2:c.1850C>T
|
NP_001334630.1:p.Ala617Val
|
|
NM_001347702.2:c.1778C>T
MANE Plus Clinical
|
NP_001334631.1:p.Ala593Val
|
|
NM_033071.5:c.25100C>T
|
NP_149062.2:p.Ala8367Val
|
|