|
NM_005633.4:c.806T>C
MANE Select
|
NP_005624.2:p.Met269Thr
|
|
ENST00000402219.8:c.806T>C
MANE Select
|
ENSP00000384675.2:p.Met269Thr
|
|
NM_001382394.1:c.785T>C
|
NP_001369323.1:p.Met262Thr
|
|
NM_001382395.1:c.806T>C
|
NP_001369324.1:p.Met269Thr
|
|
NM_005633.3:c.806T>C , LRG_754t1:c.806T>C
|
NP_005624.2:p.Met269Thr
|
|
ENST00000395038.6:c.806T>C
|
ENSP00000378479.2:p.Met269Thr
|
|
ENST00000402219.6:c.806T>C
|
ENSP00000384675.2:p.Met269Thr
|
|
ENST00000426016.5:c.806T>C
|
ENSP00000387784.1:p.Met269Thr
|
|
ENST00000461545.1:n.156T>C
|
|
|
ENST00000461545.2:n.833T>C
|
|
|
ENST00000472480.2:n.686T>C
|
|
|
ENST00000685782.1:n.1644T>C
|
|
|
ENST00000689668.1:n.813T>C
|
|
|
ENST00000690679.1:c.906T>C
|
|
|
ENST00000690876.1:c.806T>C
|
ENSP00000508955.1:p.Met269Thr
|
|
ENST00000691229.1:c.806T>C
|
ENSP00000510437.1:p.Met269Thr
|
|
ENST00000692089.1:c.806T>C
|
ENSP00000508626.1:p.Met269Thr
|
|
XM_005264515.3:c.806T>C
|
XP_005264572.1:p.Met269Thr
|
|
XM_005264515.4:c.806T>C
|
XP_005264572.1:p.Met269Thr
|
|
XM_011533060.1:c.899T>C
|
XP_011531362.1:p.Met300Thr
|
|
XM_011533061.1:c.899T>C
|
XP_011531363.1:p.Met300Thr
|
|
XM_011533062.1:c.785T>C
|
XP_011531364.1:p.Met262Thr
|
|
XM_011533062.2:c.785T>C
|
XP_011531364.1:p.Met262Thr
|
|
XM_011533063.1:c.782T>C
|
XP_011531365.1:p.Met261Thr
|
|
XM_011533064.1:c.635T>C
|
XP_011531366.1:p.Met212Thr
|
|
XM_011533064.2:c.635T>C
|
XP_011531366.1:p.Met212Thr
|
|
XM_011533065.1:c.899T>C
|
XP_011531367.1:p.Met300Thr
|
