ENST00000354674.5:c.1964C>G
MANE Plus Clinical
|
ENSP00000346701.4:p.Thr655Ser
|
|
ENST00000367255.10:c.25430C>G
MANE Select
|
ENSP00000356224.5:p.Thr8477Ser
|
|
ENST00000423061.6:c.25286C>G
|
ENSP00000396024.1:p.Thr8429Ser
|
|
ENST00000672154.1:c.832C>G
|
|
|
ENST00000672169.1:c.1165C>G
|
|
|
ENST00000673173.1:c.1074C>G
|
|
|
ENST00000673451.1:c.1202C>G
|
ENSP00000500189.1:p.Thr401Ser
|
|
ENST00000341594.9:c.24215C>G
|
ENSP00000341887.6:p.Thr8072Ser
|
|
ENST00000347037.9:n.2178C>G
|
|
|
ENST00000354674.4:c.1964C>G
|
ENSP00000346701.4:p.Thr655Ser
|
|
ENST00000367251.7:c.4265C>G
|
ENSP00000356220.3:p.Thr1422Ser
|
|
ENST00000367255.9:c.25430C>G
|
ENSP00000356224.5:p.Thr8477Ser
|
|
ENST00000367256.9:n.9122C>G
|
|
|
ENST00000367257.8:c.3368C>G
|
ENSP00000356226.4:p.Thr1123Ser
|
|
ENST00000409694.6:n.9014C>G
|
|
|
ENST00000423061.5:c.25286C>G
|
ENSP00000396024.1:p.Thr8429Ser
|
|
ENST00000460912.6:n.2044C>G
|
|
|
ENST00000478916.5:n.4452C>G
|
|
|
ENST00000536990.5:n.2267C>G
|
|
|
ENST00000539504.5:c.1895C>G
|
ENSP00000441052.1:p.Thr632Ser
|
|
NM_033071.3:c.25286C>G
|
NP_149062.1:p.Thr8429Ser
|
|
NM_182961.3:c.25430C>G
|
NP_892006.3:p.Thr8477Ser
|
|
XM_006715407.1:c.25535C>G
|
XP_006715470.1:p.Thr8512Ser
|
|
XM_006715408.1:c.25523C>G
|
XP_006715471.1:p.Thr8508Ser
|
|
XM_006715409.1:c.25514C>G
|
XP_006715472.1:p.Thr8505Ser
|
|
XM_006715410.1:c.25535C>G
|
XP_006715473.1:p.Thr8512Ser
|
|
XM_006715411.1:c.25484C>G
|
XP_006715474.1:p.Thr8495Ser
|
|
XM_006715412.1:c.25520C>G
|
XP_006715475.1:p.Thr8507Ser
|
|
XM_006715413.1:c.25466C>G
|
XP_006715476.1:p.Thr8489Ser
|
|
XM_006715414.1:c.25463C>G
|
XP_006715477.1:p.Thr8488Ser
|
|
XM_006715415.1:c.25466C>G
|
XP_006715478.1:p.Thr8489Ser
|
|
XM_006715416.1:c.25451C>G
|
XP_006715479.1:p.Thr8484Ser
|
|
XM_006715417.1:c.25394C>G
|
XP_006715480.1:p.Thr8465Ser
|
|
XM_006715420.1:c.25382C>G
|
XP_006715483.1:p.Thr8461Ser
|
|
XM_006715421.1:c.25379C>G
|
XP_006715484.1:p.Thr8460Ser
|
|
XM_006715422.1:c.25376C>G
|
XP_006715485.1:p.Thr8459Ser
|
|
XM_006715423.1:c.25535C>G
|
XP_006715486.1:p.Thr8512Ser
|
|
XM_006715424.1:c.25535C>G
|
XP_006715487.1:p.Thr8512Ser
|
|
XM_006715425.1:c.25466C>G
|
XP_006715488.1:p.Thr8489Ser
|
|
XM_011535641.1:c.25532C>G
|
XP_011533943.1:p.Thr8511Ser
|
|
XM_011535642.1:c.25520C>G
|
XP_011533944.1:p.Thr8507Ser
|
|
XM_011535643.1:c.25370C>G
|
XP_011533945.1:p.Thr8457Ser
|
|
XM_011535644.1:c.23810C>G
|
XP_011533946.1:p.Thr7937Ser
|
|
XM_011535645.1:c.23303C>G
|
XP_011533947.1:p.Thr7768Ser
|
|
XM_011535647.1:c.18770C>G
|
XP_011533949.1:p.Thr6257Ser
|
|
NM_001347701.1:c.2036C>G
|
NP_001334630.1:p.Thr679Ser
|
|
NM_001347702.1:c.1964C>G
|
NP_001334631.1:p.Thr655Ser
|
|
XM_006715408.2:c.25523C>G
|
XP_006715471.1:p.Thr8508Ser
|
|
XM_006715410.2:c.25535C>G
|
XP_006715473.1:p.Thr8512Ser
|
|
XM_006715412.2:c.25520C>G
|
XP_006715475.1:p.Thr8507Ser
|
|
XM_006715413.2:c.25466C>G
|
XP_006715476.1:p.Thr8489Ser
|
|
XM_006715415.2:c.25466C>G
|
XP_006715478.1:p.Thr8489Ser
|
|
XM_006715416.2:c.25451C>G
|
XP_006715479.1:p.Thr8484Ser
|
|
XM_006715417.2:c.25394C>G
|
XP_006715480.1:p.Thr8465Ser
|
|
XM_006715420.2:c.25382C>G
|
XP_006715483.1:p.Thr8461Ser
|
|
XM_006715421.2:c.25379C>G
|
XP_006715484.1:p.Thr8460Ser
|
|
XM_006715423.2:c.25535C>G
|
XP_006715486.1:p.Thr8512Ser
|
|
XM_006715424.2:c.25535C>G
|
XP_006715487.1:p.Thr8512Ser
|
|
XM_006715425.2:c.25466C>G
|
XP_006715488.1:p.Thr8489Ser
|
|
XM_011535641.2:c.25532C>G
|
XP_011533943.1:p.Thr8511Ser
|
|
XM_011535642.2:c.25520C>G
|
XP_011533944.1:p.Thr8507Ser
|
|
XM_011535645.2:c.23303C>G
|
XP_011533947.1:p.Thr7768Ser
|
|
XM_017010608.1:c.25535C>G
|
XP_016866097.1:p.Thr8512Ser
|
|
XM_017010609.1:c.25535C>G
|
XP_016866098.1:p.Thr8512Ser
|
|
XM_017010610.1:c.25514C>G
|
XP_016866099.1:p.Thr8505Ser
|
|
XM_017010611.2:c.25508C>G
|
XP_016866100.1:p.Thr8503Ser
|
|
XM_017010612.1:c.25457C>G
|
XP_016866101.1:p.Thr8486Ser
|
|
XM_017010613.1:c.25463C>G
|
XP_016866102.1:p.Thr8488Ser
|
|
XM_017010614.1:c.25379C>G
|
XP_016866103.1:p.Thr8460Ser
|
|
XM_017010615.1:c.25310C>G
|
XP_016866104.1:p.Thr8437Ser
|
|
XM_017010616.1:c.25466C>G
|
XP_016866105.1:p.Thr8489Ser
|
|
XM_017010617.1:c.25463C>G
|
XP_016866106.1:p.Thr8488Ser
|
|
XM_017010618.1:c.25451C>G
|
XP_016866107.1:p.Thr8484Ser
|
|
XM_017010619.1:c.23810C>G
|
XP_016866108.1:p.Thr7937Ser
|
|
NM_182961.4:c.25430C>G
MANE Select
|
NP_892006.3:p.Thr8477Ser
|
|
NM_001347701.2:c.2036C>G
|
NP_001334630.1:p.Thr679Ser
|
|
NM_001347702.2:c.1964C>G
MANE Plus Clinical
|
NP_001334631.1:p.Thr655Ser
|
|
NM_033071.5:c.25286C>G
|
NP_149062.2:p.Thr8429Ser
|
|