|
ENST00000472480.2:n.1539G=
|
|
|
|
ENST00000685279.1:c.426G=
|
ENSP00000509424.1:p.Met142=
|
|
|
ENST00000688043.1:n.1880G=
|
|
|
|
ENST00000689668.1:n.1666G=
|
|
|
|
ENST00000690876.1:c.1548G=
|
ENSP00000508955.1:p.Met516=
|
|
|
ENST00000691229.1:c.1548G=
|
ENSP00000510437.1:p.Met516=
|
|
|
ENST00000692089.1:c.1548G=
|
ENSP00000508626.1:p.Met516=
|
|
|
ENST00000692620.1:c.426G=
|
ENSP00000509311.1:p.Met142=
|
|
|
ENST00000402219.8:c.1659G=
MANE Select
|
ENSP00000384675.2:p.Met553=
|
|
|
ENST00000395038.6:c.1659G=
|
ENSP00000378479.2:p.Met553=
|
|
|
ENST00000402219.6:c.1659G=
|
ENSP00000384675.2:p.Met553=
|
|
|
ENST00000426016.5:c.1659G=
|
ENSP00000387784.1:p.Met553=
|
|
|
NM_005633.3:c.1659G= , LRG_754t1:c.1659G=
|
NP_005624.2:p.Met553=
|
|
|
XM_005264515.3:c.1659G=
|
XP_005264572.1:p.Met553=
|
|
|
XM_011533060.1:c.1752G=
|
XP_011531362.1:p.Met584=
|
|
|
XM_011533061.1:c.1752G=
|
XP_011531363.1:p.Met584=
|
|
|
XM_011533062.1:c.1638G=
|
XP_011531364.1:p.Met546=
|
|
|
XM_011533063.1:c.1635G=
|
XP_011531365.1:p.Met545=
|
|
|
XM_011533064.1:c.1488G=
|
XP_011531366.1:p.Met496=
|
|
|
XM_011533065.1:c.1752G=
|
XP_011531367.1:p.Met584=
|
|
|
XM_011533066.1:c.594G=
|
XP_011531368.1:p.Met198=
|
|
|
XM_005264515.4:c.1659G=
|
XP_005264572.1:p.Met553=
|
|
|
XM_011533062.2:c.1638G=
|
XP_011531364.1:p.Met546=
|
|
|
XM_011533064.2:c.1488G=
|
XP_011531366.1:p.Met496=
|
|
|
NM_001382394.1:c.1638G=
|
NP_001369323.1:p.Met546=
|
|
|
NM_001382395.1:c.1659G=
|
NP_001369324.1:p.Met553=
|
|
|
NM_005633.4:c.1659G=
MANE Select
|
NP_005624.2:p.Met553=
|
|
