|
ENST00000472480.2:n.1752_1758delinsAGTTGCC
|
|
|
|
ENST00000685279.1:c.625+14_625+20delinsAGTTGCC
|
ENSP00000509424.1:n.625+14_625+20delinsAGTTGCC
|
|
|
ENST00000688043.1:n.2079+14_2079+20delinsAGTTGCC
|
|
|
|
ENST00000689668.1:n.1865+14_1865+20delinsAGTTGCC
|
|
|
|
ENST00000690876.1:c.1747+14_1747+20delinsAGTTGCC
|
ENSP00000508955.1:n.1747+14_1747+20delinsAGTTGCC
|
|
|
ENST00000691229.1:c.1747+14_1747+20delinsAGTTGCC
|
ENSP00000510437.1:n.1747+14_1747+20delinsAGTTGCC
|
|
|
ENST00000692089.1:c.1747+14_1747+20delinsAGTTGCC
|
ENSP00000508626.1:n.1747+14_1747+20delinsAGTTGCC
|
|
|
ENST00000692620.1:c.625+14_625+20delinsAGTTGCC
|
ENSP00000509311.1:n.625+14_625+20delinsAGTTGCC
|
|
|
ENST00000402219.8:c.1858+14_1858+20delinsAGTTGCC
MANE Select
|
ENSP00000384675.2:n.1858+14_1858+20delinsAGTTGCC
|
|
|
ENST00000395038.6:c.1858+14_1858+20delinsAGTTGCC
|
ENSP00000378479.2:n.1858+14_1858+20delinsAGTTGCC
|
|
|
ENST00000402219.6:c.1858+14_1858+20delinsAGTTGCC
|
ENSP00000384675.2:n.1858+14_1858+20delinsAGTTGCC
|
|
|
ENST00000426016.5:c.1858+14_1858+20delinsAGTTGCC
|
ENSP00000387784.1:n.1858+14_1858+20delinsAGTTGCC
|
|
|
NM_005633.3:c.1858+14_1858+20delinsAGTTGCC , LRG_754t1:c.1858+14_1858+20delinsAGTTGCC
|
NP_005624.2:n.1858+14_1858+20delinsAGTTGCC
|
|
|
XM_005264515.3:c.1858+14_1858+20delinsAGTTGCC
|
XP_005264572.1:n.1858+14_1858+20delinsAGTTGCC
|
|
|
XM_011533060.1:c.1951+14_1951+20delinsAGTTGCC
|
XP_011531362.1:n.1951+14_1951+20delinsAGTTGCC
|
|
|
XM_011533061.1:c.1951+14_1951+20delinsAGTTGCC
|
XP_011531363.1:n.1951+14_1951+20delinsAGTTGCC
|
|
|
XM_011533062.1:c.1837+14_1837+20delinsAGTTGCC
|
XP_011531364.1:n.1837+14_1837+20delinsAGTTGCC
|
|
|
XM_011533063.1:c.1834+14_1834+20delinsAGTTGCC
|
XP_011531365.1:n.1834+14_1834+20delinsAGTTGCC
|
|
|
XM_011533064.1:c.1687+14_1687+20delinsAGTTGCC
|
XP_011531366.1:n.1687+14_1687+20delinsAGTTGCC
|
|
|
XM_011533065.1:c.1951+14_1951+20delinsAGTTGCC
|
XP_011531367.1:n.1951+14_1951+20delinsAGTTGCC
|
|
|
XM_011533066.1:c.793+14_793+20delinsAGTTGCC
|
XP_011531368.1:n.793+14_793+20delinsAGTTGCC
|
|
|
XM_005264515.4:c.1858+14_1858+20delinsAGTTGCC
|
XP_005264572.1:n.1858+14_1858+20delinsAGTTGCC
|
|
|
XM_011533062.2:c.1837+14_1837+20delinsAGTTGCC
|
XP_011531364.1:n.1837+14_1837+20delinsAGTTGCC
|
|
|
XM_011533064.2:c.1687+14_1687+20delinsAGTTGCC
|
XP_011531366.1:n.1687+14_1687+20delinsAGTTGCC
|
|
|
NM_001382394.1:c.1837+14_1837+20delinsAGTTGCC
|
NP_001369323.1:n.1837+14_1837+20delinsAGTTGCC
|
|
|
NM_001382395.1:c.1858+14_1858+20delinsAGTTGCC
|
NP_001369324.1:n.1858+14_1858+20delinsAGTTGCC
|
|
|
NM_005633.4:c.1858+14_1858+20delinsAGTTGCC
MANE Select
|
NP_005624.2:n.1858+14_1858+20delinsAGTTGCC
|
|
