ENST00000354674.5:c.1815G>T
MANE Plus Clinical
|
ENSP00000346701.4:p.Gln605His
|
|
ENST00000367255.10:c.25281G>T
MANE Select
|
ENSP00000356224.5:p.Gln8427His
|
|
ENST00000423061.6:c.25137G>T
|
ENSP00000396024.1:p.Gln8379His
|
|
ENST00000672154.1:c.683G>T
|
|
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ENST00000672169.1:c.1016G>T
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|
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ENST00000673173.1:c.925G>T
|
|
|
ENST00000673451.1:c.1053G>T
|
ENSP00000500189.1:p.Gln351His
|
|
ENST00000341594.9:c.24066G>T
|
ENSP00000341887.6:p.Gln8022His
|
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ENST00000347037.9:n.2029G>T
|
|
|
ENST00000354674.4:c.1815G>T
|
ENSP00000346701.4:p.Gln605His
|
|
ENST00000367251.7:c.4116G>T
|
ENSP00000356220.3:p.Gln1372His
|
|
ENST00000367255.9:c.25281G>T
|
ENSP00000356224.5:p.Gln8427His
|
|
ENST00000367256.9:n.8973G>T
|
|
|
ENST00000367257.8:c.3219G>T
|
ENSP00000356226.4:p.Gln1073His
|
|
ENST00000409694.6:n.8865G>T
|
|
|
ENST00000423061.5:c.25137G>T
|
ENSP00000396024.1:p.Gln8379His
|
|
ENST00000460912.6:n.1895G>T
|
|
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ENST00000478916.5:n.4303G>T
|
|
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ENST00000536990.5:n.2118G>T
|
|
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ENST00000539504.5:c.1746G>T
|
ENSP00000441052.1:p.Gln582His
|
|
NM_033071.3:c.25137G>T
|
NP_149062.1:p.Gln8379His
|
|
NM_182961.3:c.25281G>T
|
NP_892006.3:p.Gln8427His
|
|
XM_006715407.1:c.25386G>T
|
XP_006715470.1:p.Gln8462His
|
|
XM_006715408.1:c.25374G>T
|
XP_006715471.1:p.Gln8458His
|
|
XM_006715409.1:c.25365G>T
|
XP_006715472.1:p.Gln8455His
|
|
XM_006715410.1:c.25386G>T
|
XP_006715473.1:p.Gln8462His
|
|
XM_006715411.1:c.25335G>T
|
XP_006715474.1:p.Gln8445His
|
|
XM_006715412.1:c.25371G>T
|
XP_006715475.1:p.Gln8457His
|
|
XM_006715413.1:c.25317G>T
|
XP_006715476.1:p.Gln8439His
|
|
XM_006715414.1:c.25314G>T
|
XP_006715477.1:p.Gln8438His
|
|
XM_006715415.1:c.25317G>T
|
XP_006715478.1:p.Gln8439His
|
|
XM_006715416.1:c.25302G>T
|
XP_006715479.1:p.Gln8434His
|
|
XM_006715417.1:c.25245G>T
|
XP_006715480.1:p.Gln8415His
|
|
XM_006715420.1:c.25233G>T
|
XP_006715483.1:p.Gln8411His
|
|
XM_006715421.1:c.25230G>T
|
XP_006715484.1:p.Gln8410His
|
|
XM_006715422.1:c.25227G>T
|
XP_006715485.1:p.Gln8409His
|
|
XM_006715423.1:c.25386G>T
|
XP_006715486.1:p.Gln8462His
|
|
XM_006715424.1:c.25386G>T
|
XP_006715487.1:p.Gln8462His
|
|
XM_006715425.1:c.25317G>T
|
XP_006715488.1:p.Gln8439His
|
|
XM_011535641.1:c.25383G>T
|
XP_011533943.1:p.Gln8461His
|
|
XM_011535642.1:c.25371G>T
|
XP_011533944.1:p.Gln8457His
|
|
XM_011535643.1:c.25221G>T
|
XP_011533945.1:p.Gln8407His
|
|
XM_011535644.1:c.23661G>T
|
XP_011533946.1:p.Gln7887His
|
|
XM_011535645.1:c.23154G>T
|
XP_011533947.1:p.Gln7718His
|
|
XM_011535647.1:c.18621G>T
|
XP_011533949.1:p.Gln6207His
|
|
NM_001347701.1:c.1887G>T
|
NP_001334630.1:p.Gln629His
|
|
NM_001347702.1:c.1815G>T
|
NP_001334631.1:p.Gln605His
|
|
XM_006715408.2:c.25374G>T
|
XP_006715471.1:p.Gln8458His
|
|
XM_006715410.2:c.25386G>T
|
XP_006715473.1:p.Gln8462His
|
|
XM_006715412.2:c.25371G>T
|
XP_006715475.1:p.Gln8457His
|
|
XM_006715413.2:c.25317G>T
|
XP_006715476.1:p.Gln8439His
|
|
XM_006715415.2:c.25317G>T
|
XP_006715478.1:p.Gln8439His
|
|
XM_006715416.2:c.25302G>T
|
XP_006715479.1:p.Gln8434His
|
|
XM_006715417.2:c.25245G>T
|
XP_006715480.1:p.Gln8415His
|
|
XM_006715420.2:c.25233G>T
|
XP_006715483.1:p.Gln8411His
|
|
XM_006715421.2:c.25230G>T
|
XP_006715484.1:p.Gln8410His
|
|
XM_006715423.2:c.25386G>T
|
XP_006715486.1:p.Gln8462His
|
|
XM_006715424.2:c.25386G>T
|
XP_006715487.1:p.Gln8462His
|
|
XM_006715425.2:c.25317G>T
|
XP_006715488.1:p.Gln8439His
|
|
XM_011535641.2:c.25383G>T
|
XP_011533943.1:p.Gln8461His
|
|
XM_011535642.2:c.25371G>T
|
XP_011533944.1:p.Gln8457His
|
|
XM_011535645.2:c.23154G>T
|
XP_011533947.1:p.Gln7718His
|
|
XM_017010608.1:c.25386G>T
|
XP_016866097.1:p.Gln8462His
|
|
XM_017010609.1:c.25386G>T
|
XP_016866098.1:p.Gln8462His
|
|
XM_017010610.1:c.25365G>T
|
XP_016866099.1:p.Gln8455His
|
|
XM_017010611.2:c.25359G>T
|
XP_016866100.1:p.Gln8453His
|
|
XM_017010612.1:c.25308G>T
|
XP_016866101.1:p.Gln8436His
|
|
XM_017010613.1:c.25314G>T
|
XP_016866102.1:p.Gln8438His
|
|
XM_017010614.1:c.25230G>T
|
XP_016866103.1:p.Gln8410His
|
|
XM_017010615.1:c.25161G>T
|
XP_016866104.1:p.Gln8387His
|
|
XM_017010616.1:c.25317G>T
|
XP_016866105.1:p.Gln8439His
|
|
XM_017010617.1:c.25314G>T
|
XP_016866106.1:p.Gln8438His
|
|
XM_017010618.1:c.25302G>T
|
XP_016866107.1:p.Gln8434His
|
|
XM_017010619.1:c.23661G>T
|
XP_016866108.1:p.Gln7887His
|
|
NM_182961.4:c.25281G>T
MANE Select
|
NP_892006.3:p.Gln8427His
|
|
NM_001347701.2:c.1887G>T
|
NP_001334630.1:p.Gln629His
|
|
NM_001347702.2:c.1815G>T
MANE Plus Clinical
|
NP_001334631.1:p.Gln605His
|
|
NM_033071.5:c.25137G>T
|
NP_149062.2:p.Gln8379His
|
|