|
ENST00000684779.1:c.628-2056C>T
|
ENSP00000508681.1:n.628-2056C>T
|
|
|
ENST00000685172.1:c.876C>T
|
ENSP00000509604.1:p.Thr292=
|
|
|
ENST00000685763.1:c.729C>T
|
ENSP00000509016.1:p.Thr243=
|
|
|
ENST00000686347.1:c.569-2056C>T
|
ENSP00000509027.1:n.569-2056C>T
|
|
|
ENST00000687191.1:n.1234C>T
|
|
|
|
ENST00000687481.1:n.291C>T
|
|
|
|
ENST00000689951.1:c.927C>T
|
ENSP00000509308.1:p.Thr309=
|
|
|
ENST00000691077.1:c.*113C>T
|
ENSP00000509843.1:n.*113C>T
|
|
|
ENST00000691576.1:c.747C>T
|
ENSP00000510066.1:p.Thr249=
|
|
|
ENST00000691937.1:c.876C>T
|
ENSP00000508768.1:p.Thr292=
|
|
|
ENST00000692487.1:c.*113C>T
|
ENSP00000509534.1:n.*113C>T
|
|
|
ENST00000692683.1:c.810C>T
|
ENSP00000508437.1:p.Thr270=
|
|
|
ENST00000693150.1:c.732C>T
|
ENSP00000510309.1:p.Thr244=
|
|
|
ENST00000307102.10:c.876C>T
MANE Select
|
ENSP00000302486.5:p.Thr292=
|
|
|
ENST00000307102.9:c.876C>T
|
ENSP00000302486.4:p.Thr292=
|
|
|
ENST00000566326.1:c.348C>T
|
ENSP00000456438.1:p.Thr116=
|
|
|
NM_002755.3:c.876C>T , LRG_725t1:c.876C>T
|
NP_002746.1:p.Thr292=
|
|
|
XM_011521783.1:c.810C>T
|
XP_011520085.1:p.Thr270=
|
|
|
XM_011521783.3:c.810C>T
|
XP_011520085.1:p.Thr270=
|
|
|
XM_017022411.2:c.798C>T
|
XP_016877900.1:p.Thr266=
|
|
|
XM_017022412.1:c.732C>T
|
XP_016877901.1:p.Thr244=
|
|
|
XM_017022413.1:c.348C>T
|
XP_016877902.1:p.Thr116=
|
|
|
NM_002755.4:c.876C>T
MANE Select
|
NP_002746.1:p.Thr292=
|
|
