ENST00000354674.5:c.1685T>C
MANE Plus Clinical
|
ENSP00000346701.4:p.Ile562Thr
|
|
ENST00000367255.10:c.25151T>C
MANE Select
|
ENSP00000356224.5:p.Ile8384Thr
|
|
ENST00000423061.6:c.25007T>C
|
ENSP00000396024.1:p.Ile8336Thr
|
|
ENST00000672154.1:c.553T>C
|
|
|
ENST00000672169.1:c.886T>C
|
|
|
ENST00000673173.1:c.891-1137T>C
|
|
|
ENST00000673451.1:c.923T>C
|
ENSP00000500189.1:p.Ile308Thr
|
|
ENST00000341594.9:c.23936T>C
|
ENSP00000341887.6:p.Ile7979Thr
|
|
ENST00000347037.9:n.1899T>C
|
|
|
ENST00000354674.4:c.1685T>C
|
ENSP00000346701.4:p.Ile562Thr
|
|
ENST00000367251.7:c.3986T>C
|
ENSP00000356220.3:p.Ile1329Thr
|
|
ENST00000367255.9:c.25151T>C
|
ENSP00000356224.5:p.Ile8384Thr
|
|
ENST00000367256.9:n.8843T>C
|
|
|
ENST00000367257.8:c.3089T>C
|
ENSP00000356226.4:p.Ile1030Thr
|
|
ENST00000409694.6:n.8735T>C
|
|
|
ENST00000423061.5:c.25007T>C
|
ENSP00000396024.1:p.Ile8336Thr
|
|
ENST00000460912.6:n.1765T>C
|
|
|
ENST00000478916.5:n.4173T>C
|
|
|
ENST00000536990.5:n.1988T>C
|
|
|
ENST00000539504.5:c.1616T>C
|
ENSP00000441052.1:p.Ile539Thr
|
|
NM_033071.3:c.25007T>C
|
NP_149062.1:p.Ile8336Thr
|
|
NM_182961.3:c.25151T>C
|
NP_892006.3:p.Ile8384Thr
|
|
XM_006715407.1:c.25256T>C
|
XP_006715470.1:p.Ile8419Thr
|
|
XM_006715408.1:c.25244T>C
|
XP_006715471.1:p.Ile8415Thr
|
|
XM_006715409.1:c.25235T>C
|
XP_006715472.1:p.Ile8412Thr
|
|
XM_006715410.1:c.25256T>C
|
XP_006715473.1:p.Ile8419Thr
|
|
XM_006715411.1:c.25205T>C
|
XP_006715474.1:p.Ile8402Thr
|
|
XM_006715412.1:c.25241T>C
|
XP_006715475.1:p.Ile8414Thr
|
|
XM_006715413.1:c.25187T>C
|
XP_006715476.1:p.Ile8396Thr
|
|
XM_006715414.1:c.25184T>C
|
XP_006715477.1:p.Ile8395Thr
|
|
XM_006715415.1:c.25187T>C
|
XP_006715478.1:p.Ile8396Thr
|
|
XM_006715416.1:c.25172T>C
|
XP_006715479.1:p.Ile8391Thr
|
|
XM_006715417.1:c.25115T>C
|
XP_006715480.1:p.Ile8372Thr
|
|
XM_006715420.1:c.25103T>C
|
XP_006715483.1:p.Ile8368Thr
|
|
XM_006715421.1:c.25100T>C
|
XP_006715484.1:p.Ile8367Thr
|
|
XM_006715422.1:c.25097T>C
|
XP_006715485.1:p.Ile8366Thr
|
|
XM_006715423.1:c.25256T>C
|
XP_006715486.1:p.Ile8419Thr
|
|
XM_006715424.1:c.25256T>C
|
XP_006715487.1:p.Ile8419Thr
|
|
XM_006715425.1:c.25187T>C
|
XP_006715488.1:p.Ile8396Thr
|
|
XM_011535641.1:c.25253T>C
|
XP_011533943.1:p.Ile8418Thr
|
|
XM_011535642.1:c.25241T>C
|
XP_011533944.1:p.Ile8414Thr
|
|
XM_011535643.1:c.25091T>C
|
XP_011533945.1:p.Ile8364Thr
|
|
XM_011535644.1:c.23531T>C
|
XP_011533946.1:p.Ile7844Thr
|
|
XM_011535645.1:c.23024T>C
|
XP_011533947.1:p.Ile7675Thr
|
|
XM_011535647.1:c.18491T>C
|
XP_011533949.1:p.Ile6164Thr
|
|
NM_001347701.1:c.1757T>C
|
NP_001334630.1:p.Ile586Thr
|
|
NM_001347702.1:c.1685T>C
|
NP_001334631.1:p.Ile562Thr
|
|
XM_006715408.2:c.25244T>C
|
XP_006715471.1:p.Ile8415Thr
|
|
XM_006715410.2:c.25256T>C
|
XP_006715473.1:p.Ile8419Thr
|
|
XM_006715412.2:c.25241T>C
|
XP_006715475.1:p.Ile8414Thr
|
|
XM_006715413.2:c.25187T>C
|
XP_006715476.1:p.Ile8396Thr
|
|
XM_006715415.2:c.25187T>C
|
XP_006715478.1:p.Ile8396Thr
|
|
XM_006715416.2:c.25172T>C
|
XP_006715479.1:p.Ile8391Thr
|
|
XM_006715417.2:c.25115T>C
|
XP_006715480.1:p.Ile8372Thr
|
|
XM_006715420.2:c.25103T>C
|
XP_006715483.1:p.Ile8368Thr
|
|
XM_006715421.2:c.25100T>C
|
XP_006715484.1:p.Ile8367Thr
|
|
XM_006715423.2:c.25256T>C
|
XP_006715486.1:p.Ile8419Thr
|
|
XM_006715424.2:c.25256T>C
|
XP_006715487.1:p.Ile8419Thr
|
|
XM_006715425.2:c.25187T>C
|
XP_006715488.1:p.Ile8396Thr
|
|
XM_011535641.2:c.25253T>C
|
XP_011533943.1:p.Ile8418Thr
|
|
XM_011535642.2:c.25241T>C
|
XP_011533944.1:p.Ile8414Thr
|
|
XM_011535645.2:c.23024T>C
|
XP_011533947.1:p.Ile7675Thr
|
|
XM_017010608.1:c.25256T>C
|
XP_016866097.1:p.Ile8419Thr
|
|
XM_017010609.1:c.25256T>C
|
XP_016866098.1:p.Ile8419Thr
|
|
XM_017010610.1:c.25235T>C
|
XP_016866099.1:p.Ile8412Thr
|
|
XM_017010611.2:c.25229T>C
|
XP_016866100.1:p.Ile8410Thr
|
|
XM_017010612.1:c.25178T>C
|
XP_016866101.1:p.Ile8393Thr
|
|
XM_017010613.1:c.25184T>C
|
XP_016866102.1:p.Ile8395Thr
|
|
XM_017010614.1:c.25100T>C
|
XP_016866103.1:p.Ile8367Thr
|
|
XM_017010615.1:c.25031T>C
|
XP_016866104.1:p.Ile8344Thr
|
|
XM_017010616.1:c.25187T>C
|
XP_016866105.1:p.Ile8396Thr
|
|
XM_017010617.1:c.25184T>C
|
XP_016866106.1:p.Ile8395Thr
|
|
XM_017010618.1:c.25172T>C
|
XP_016866107.1:p.Ile8391Thr
|
|
XM_017010619.1:c.23531T>C
|
XP_016866108.1:p.Ile7844Thr
|
|
NM_182961.4:c.25151T>C
MANE Select
|
NP_892006.3:p.Ile8384Thr
|
|
NM_001347701.2:c.1757T>C
|
NP_001334630.1:p.Ile586Thr
|
|
NM_001347702.2:c.1685T>C
MANE Plus Clinical
|
NP_001334631.1:p.Ile562Thr
|
|
NM_033071.5:c.25007T>C
|
NP_149062.2:p.Ile8336Thr
|
|