|
NM_005633.4:c.3322G>A
MANE Select
|
NP_005624.2:p.Asp1108Asn
|
|
ENST00000402219.8:c.3322G>A
MANE Select
|
ENSP00000384675.2:p.Asp1108Asn
|
|
NM_001382394.1:c.3301G>A
|
NP_001369323.1:p.Asp1101Asn
|
|
NM_001382395.1:c.3322G>A
|
NP_001369324.1:p.Asp1108Asn
|
|
NM_005633.3:c.3322G>A , LRG_754t1:c.3322G>A
|
NP_005624.2:p.Asp1108Asn
|
|
ENST00000395038.6:c.3322G>A
|
ENSP00000378479.2:p.Asp1108Asn
|
|
ENST00000402219.6:c.3322G>A
|
ENSP00000384675.2:p.Asp1108Asn
|
|
ENST00000426016.5:c.3322G>A
|
ENSP00000387784.1:p.Asp1108Asn
|
|
ENST00000685279.1:c.2089G>A
|
ENSP00000509424.1:p.Asp697Asn
|
|
ENST00000690876.1:c.*628G>A
|
ENSP00000508955.1:n.*628G>A
|
|
ENST00000691229.1:c.3091G>A
|
ENSP00000510437.1:p.Asp1031Asn
|
|
ENST00000692089.1:c.3211G>A
|
ENSP00000508626.1:p.Asp1071Asn
|
|
ENST00000692227.1:c.1018G>A
|
ENSP00000509138.1:p.Asp340Asn
|
|
ENST00000692620.1:c.*909G>A
|
ENSP00000509311.1:n.*909G>A
|
|
XM_005264515.3:c.3322G>A
|
XP_005264572.1:p.Asp1108Asn
|
|
XM_005264515.4:c.3322G>A
|
XP_005264572.1:p.Asp1108Asn
|
|
XM_011533060.1:c.3415G>A
|
XP_011531362.1:p.Asp1139Asn
|
|
XM_011533061.1:c.3415G>A
|
XP_011531363.1:p.Asp1139Asn
|
|
XM_011533062.1:c.3301G>A
|
XP_011531364.1:p.Asp1101Asn
|
|
XM_011533062.2:c.3301G>A
|
XP_011531364.1:p.Asp1101Asn
|
|
XM_011533063.1:c.3298G>A
|
XP_011531365.1:p.Asp1100Asn
|
|
XM_011533064.1:c.3151G>A
|
XP_011531366.1:p.Asp1051Asn
|
|
XM_011533064.2:c.3151G>A
|
XP_011531366.1:p.Asp1051Asn
|
|
XM_011533065.1:c.3415G>A
|
XP_011531367.1:p.Asp1139Asn
|
|
XM_011533066.1:c.2257G>A
|
XP_011531368.1:p.Asp753Asn
|
