ENST00000354674.5:c.1830G>C
MANE Plus Clinical
|
ENSP00000346701.4:p.Glu610Asp
|
|
ENST00000367255.10:c.25296G>C
MANE Select
|
ENSP00000356224.5:p.Glu8432Asp
|
|
ENST00000423061.6:c.25152G>C
|
ENSP00000396024.1:p.Glu8384Asp
|
|
ENST00000672154.1:c.698G>C
|
|
|
ENST00000672169.1:c.1031G>C
|
|
|
ENST00000673173.1:c.940G>C
|
|
|
ENST00000673451.1:c.1068G>C
|
ENSP00000500189.1:p.Glu356Asp
|
|
ENST00000341594.9:c.24081G>C
|
ENSP00000341887.6:p.Glu8027Asp
|
|
ENST00000347037.9:n.2044G>C
|
|
|
ENST00000354674.4:c.1830G>C
|
ENSP00000346701.4:p.Glu610Asp
|
|
ENST00000367251.7:c.4131G>C
|
ENSP00000356220.3:p.Glu1377Asp
|
|
ENST00000367255.9:c.25296G>C
|
ENSP00000356224.5:p.Glu8432Asp
|
|
ENST00000367256.9:n.8988G>C
|
|
|
ENST00000367257.8:c.3234G>C
|
ENSP00000356226.4:p.Glu1078Asp
|
|
ENST00000409694.6:n.8880G>C
|
|
|
ENST00000423061.5:c.25152G>C
|
ENSP00000396024.1:p.Glu8384Asp
|
|
ENST00000460912.6:n.1910G>C
|
|
|
ENST00000478916.5:n.4318G>C
|
|
|
ENST00000536990.5:n.2133G>C
|
|
|
ENST00000539504.5:c.1761G>C
|
ENSP00000441052.1:p.Glu587Asp
|
|
NM_033071.3:c.25152G>C
|
NP_149062.1:p.Glu8384Asp
|
|
NM_182961.3:c.25296G>C
|
NP_892006.3:p.Glu8432Asp
|
|
XM_006715407.1:c.25401G>C
|
XP_006715470.1:p.Glu8467Asp
|
|
XM_006715408.1:c.25389G>C
|
XP_006715471.1:p.Glu8463Asp
|
|
XM_006715409.1:c.25380G>C
|
XP_006715472.1:p.Glu8460Asp
|
|
XM_006715410.1:c.25401G>C
|
XP_006715473.1:p.Glu8467Asp
|
|
XM_006715411.1:c.25350G>C
|
XP_006715474.1:p.Glu8450Asp
|
|
XM_006715412.1:c.25386G>C
|
XP_006715475.1:p.Glu8462Asp
|
|
XM_006715413.1:c.25332G>C
|
XP_006715476.1:p.Glu8444Asp
|
|
XM_006715414.1:c.25329G>C
|
XP_006715477.1:p.Glu8443Asp
|
|
XM_006715415.1:c.25332G>C
|
XP_006715478.1:p.Glu8444Asp
|
|
XM_006715416.1:c.25317G>C
|
XP_006715479.1:p.Glu8439Asp
|
|
XM_006715417.1:c.25260G>C
|
XP_006715480.1:p.Glu8420Asp
|
|
XM_006715420.1:c.25248G>C
|
XP_006715483.1:p.Glu8416Asp
|
|
XM_006715421.1:c.25245G>C
|
XP_006715484.1:p.Glu8415Asp
|
|
XM_006715422.1:c.25242G>C
|
XP_006715485.1:p.Glu8414Asp
|
|
XM_006715423.1:c.25401G>C
|
XP_006715486.1:p.Glu8467Asp
|
|
XM_006715424.1:c.25401G>C
|
XP_006715487.1:p.Glu8467Asp
|
|
XM_006715425.1:c.25332G>C
|
XP_006715488.1:p.Glu8444Asp
|
|
XM_011535641.1:c.25398G>C
|
XP_011533943.1:p.Glu8466Asp
|
|
XM_011535642.1:c.25386G>C
|
XP_011533944.1:p.Glu8462Asp
|
|
XM_011535643.1:c.25236G>C
|
XP_011533945.1:p.Glu8412Asp
|
|
XM_011535644.1:c.23676G>C
|
XP_011533946.1:p.Glu7892Asp
|
|
XM_011535645.1:c.23169G>C
|
XP_011533947.1:p.Glu7723Asp
|
|
XM_011535647.1:c.18636G>C
|
XP_011533949.1:p.Glu6212Asp
|
|
NM_001347701.1:c.1902G>C
|
NP_001334630.1:p.Glu634Asp
|
|
NM_001347702.1:c.1830G>C
|
NP_001334631.1:p.Glu610Asp
|
|
XM_006715408.2:c.25389G>C
|
XP_006715471.1:p.Glu8463Asp
|
|
XM_006715410.2:c.25401G>C
|
XP_006715473.1:p.Glu8467Asp
|
|
XM_006715412.2:c.25386G>C
|
XP_006715475.1:p.Glu8462Asp
|
|
XM_006715413.2:c.25332G>C
|
XP_006715476.1:p.Glu8444Asp
|
|
XM_006715415.2:c.25332G>C
|
XP_006715478.1:p.Glu8444Asp
|
|
XM_006715416.2:c.25317G>C
|
XP_006715479.1:p.Glu8439Asp
|
|
XM_006715417.2:c.25260G>C
|
XP_006715480.1:p.Glu8420Asp
|
|
XM_006715420.2:c.25248G>C
|
XP_006715483.1:p.Glu8416Asp
|
|
XM_006715421.2:c.25245G>C
|
XP_006715484.1:p.Glu8415Asp
|
|
XM_006715423.2:c.25401G>C
|
XP_006715486.1:p.Glu8467Asp
|
|
XM_006715424.2:c.25401G>C
|
XP_006715487.1:p.Glu8467Asp
|
|
XM_006715425.2:c.25332G>C
|
XP_006715488.1:p.Glu8444Asp
|
|
XM_011535641.2:c.25398G>C
|
XP_011533943.1:p.Glu8466Asp
|
|
XM_011535642.2:c.25386G>C
|
XP_011533944.1:p.Glu8462Asp
|
|
XM_011535645.2:c.23169G>C
|
XP_011533947.1:p.Glu7723Asp
|
|
XM_017010608.1:c.25401G>C
|
XP_016866097.1:p.Glu8467Asp
|
|
XM_017010609.1:c.25401G>C
|
XP_016866098.1:p.Glu8467Asp
|
|
XM_017010610.1:c.25380G>C
|
XP_016866099.1:p.Glu8460Asp
|
|
XM_017010611.2:c.25374G>C
|
XP_016866100.1:p.Glu8458Asp
|
|
XM_017010612.1:c.25323G>C
|
XP_016866101.1:p.Glu8441Asp
|
|
XM_017010613.1:c.25329G>C
|
XP_016866102.1:p.Glu8443Asp
|
|
XM_017010614.1:c.25245G>C
|
XP_016866103.1:p.Glu8415Asp
|
|
XM_017010615.1:c.25176G>C
|
XP_016866104.1:p.Glu8392Asp
|
|
XM_017010616.1:c.25332G>C
|
XP_016866105.1:p.Glu8444Asp
|
|
XM_017010617.1:c.25329G>C
|
XP_016866106.1:p.Glu8443Asp
|
|
XM_017010618.1:c.25317G>C
|
XP_016866107.1:p.Glu8439Asp
|
|
XM_017010619.1:c.23676G>C
|
XP_016866108.1:p.Glu7892Asp
|
|
NM_182961.4:c.25296G>C
MANE Select
|
NP_892006.3:p.Glu8432Asp
|
|
NM_001347701.2:c.1902G>C
|
NP_001334630.1:p.Glu634Asp
|
|
NM_001347702.2:c.1830G>C
MANE Plus Clinical
|
NP_001334631.1:p.Glu610Asp
|
|
NM_033071.5:c.25152G>C
|
NP_149062.2:p.Glu8384Asp
|
|