ENST00000375687.10:c.3721G=
MANE Select
|
ENSP00000364839.4:p.Glu1241=
|
|
ENST00000646985.1:c.3538G=
|
ENSP00000495053.1:p.Glu1180=
|
|
ENST00000647223.1:n.6074G=
|
|
|
ENST00000651418.1:c.1869+1852G=
|
ENSP00000499150.1:n.1869+1852G=
|
|
ENST00000306058.9:c.3706G=
|
ENSP00000305119.5:p.Glu1236=
|
|
ENST00000375687.8:c.3721G=
|
ENSP00000364839.4:p.Glu1241=
|
|
ENST00000613218.4:c.3721G=
|
ENSP00000480487.1:p.Glu1241=
|
|
ENST00000620121.4:c.3721G=
|
ENSP00000481978.1:p.Glu1241=
|
|
NM_015338.5:c.3721G= , LRG_630t1:c.3721G=
|
NP_056153.2:p.Glu1241=
|
|
XM_006723727.2:c.3718G=
|
XP_006723790.1:p.Glu1240=
|
|
XM_006723728.2:c.3691G=
|
XP_006723791.1:p.Glu1231=
|
|
XM_006723730.2:c.3637G=
|
XP_006723793.1:p.Glu1213=
|
|
XM_006723732.2:c.3538G=
|
XP_006723795.1:p.Glu1180=
|
|
XM_006723733.1:c.3037G=
|
XP_006723796.1:p.Glu1013=
|
|
XM_011528647.1:c.3985G=
|
XP_011526949.1:p.Glu1329=
|
|
XM_011528648.1:c.3982G=
|
XP_011526950.1:p.Glu1328=
|
|
XM_011528649.1:c.3901G=
|
XP_011526951.1:p.Glu1301=
|
|
XM_011528650.1:c.3832G=
|
XP_011526952.1:p.Glu1278=
|
|
XM_011528651.1:c.3700G=
|
XP_011526953.1:p.Glu1234=
|
|
XM_011528652.1:c.3637G=
|
XP_011526954.1:p.Glu1213=
|
|
NM_001363734.1:c.3538G=
|
NP_001350663.1:p.Glu1180=
|
|
XM_006723727.3:c.3718G=
|
XP_006723790.1:p.Glu1240=
|
|
XM_006723728.3:c.3691G=
|
XP_006723791.1:p.Glu1231=
|
|
XM_006723730.4:c.3637G=
|
XP_006723793.1:p.Glu1213=
|
|
XM_011528648.3:c.3982G=
|
XP_011526950.1:p.Glu1328=
|
|
XM_011528652.2:c.3637G=
|
XP_011526954.1:p.Glu1213=
|
|
XM_017027704.1:c.3637G=
|
XP_016883193.1:p.Glu1213=
|
|
XM_017027705.1:c.3637G=
|
XP_016883194.1:p.Glu1213=
|
|
XM_017027706.1:c.3568G=
|
XP_016883195.1:p.Glu1190=
|
|
NM_015338.6:c.3721G=
MANE Select
|
NP_056153.2:p.Glu1241=
|
|