ENST00000461545.2:n.711G>T
|
|
|
ENST00000685782.1:n.1522G>T
|
|
|
ENST00000688189.1:n.449G>T
|
|
|
ENST00000689668.1:n.691G>T
|
|
|
ENST00000690679.1:c.784G>T
|
|
|
ENST00000690876.1:c.684G>T
|
ENSP00000508955.1:p.Glu228Asp
|
|
ENST00000691229.1:c.684G>T
|
ENSP00000510437.1:p.Glu228Asp
|
|
ENST00000692089.1:c.684G>T
|
ENSP00000508626.1:p.Glu228Asp
|
|
ENST00000402219.8:c.684G>T
MANE Select
|
ENSP00000384675.2:p.Glu228Asp
|
|
ENST00000395038.6:c.684G>T
|
ENSP00000378479.2:p.Glu228Asp
|
|
ENST00000402219.6:c.684G>T
|
ENSP00000384675.2:p.Glu228Asp
|
|
ENST00000426016.5:c.684G>T
|
ENSP00000387784.1:p.Glu228Asp
|
|
NM_005633.3:c.684G>T , LRG_754t1:c.684G>T
|
NP_005624.2:p.Glu228Asp
|
|
XM_005264515.3:c.684G>T
|
XP_005264572.1:p.Glu228Asp
|
|
XM_011533060.1:c.777G>T
|
XP_011531362.1:p.Glu259Asp
|
|
XM_011533061.1:c.777G>T
|
XP_011531363.1:p.Glu259Asp
|
|
XM_011533062.1:c.663G>T
|
XP_011531364.1:p.Glu221Asp
|
|
XM_011533063.1:c.660G>T
|
XP_011531365.1:p.Glu220Asp
|
|
XM_011533064.1:c.513G>T
|
XP_011531366.1:p.Glu171Asp
|
|
XM_011533065.1:c.777G>T
|
XP_011531367.1:p.Glu259Asp
|
|
XM_005264515.4:c.684G>T
|
XP_005264572.1:p.Glu228Asp
|
|
XM_011533062.2:c.663G>T
|
XP_011531364.1:p.Glu221Asp
|
|
XM_011533064.2:c.513G>T
|
XP_011531366.1:p.Glu171Asp
|
|
NM_001382394.1:c.663G>T
|
NP_001369323.1:p.Glu221Asp
|
|
NM_001382395.1:c.684G>T
|
NP_001369324.1:p.Glu228Asp
|
|
NM_005633.4:c.684G>T
MANE Select
|
NP_005624.2:p.Glu228Asp
|
|