ENST00000555675.6:n.73G>T
|
|
|
ENST00000556394.2:c.249-1631G>T
|
ENSP00000451967.2:n.249-1631G>T
|
|
ENST00000556880.6:n.277G>T
|
|
|
ENST00000682247.1:c.344G>T
|
ENSP00000507213.1:p.Gly115Val
|
|
ENST00000682382.1:c.292G>T
|
|
|
ENST00000682395.1:n.73G>T
|
|
|
ENST00000682459.1:n.73G>T
|
|
|
ENST00000682467.1:c.344G>T
|
ENSP00000508062.1:p.Gly115Val
|
|
ENST00000682795.1:c.344G>T
|
ENSP00000507574.1:p.Gly115Val
|
|
ENST00000682895.1:n.60G>T
|
|
|
ENST00000682955.1:n.73G>T
|
|
|
ENST00000683188.1:c.139G>T
|
|
|
ENST00000683380.1:n.73G>T
|
|
|
ENST00000683828.1:c.213G>T
|
|
|
ENST00000684066.1:n.39G>T
|
|
|
ENST00000684102.1:n.90G>T
|
|
|
ENST00000684259.1:n.195G>T
|
|
|
ENST00000684479.1:n.11G>T
|
|
|
ENST00000684549.1:n.73G>T
|
|
|
ENST00000684600.1:c.158G>T
|
|
|
ENST00000684670.1:n.11G>T
|
|
|
ENST00000684746.1:n.41G>T
|
|
|
ENST00000261534.9:c.344G>T
MANE Select
|
ENSP00000261534.4:p.Gly115Val
|
|
ENST00000261534.8:c.344G>T
|
ENSP00000261534.4:p.Gly115Val
|
|
ENST00000452340.7:n.367G>T
|
|
|
ENST00000553863.5:n.73G>T
|
|
|
ENST00000554948.1:c.71G>T
|
ENSP00000452060.1:p.Gly24Val
|
|
ENST00000555675.5:n.60G>T
|
|
|
ENST00000555788.5:n.178G>T
|
|
|
ENST00000556326.5:c.*10G>T
|
ENSP00000450630.1:n.*10G>T
|
|
ENST00000556880.5:n.277G>T
|
|
|
ENST00000557525.1:n.434G>T
|
|
|
NM_013382.5:c.344G>T , LRG_844t1:c.344G>T
|
NP_037514.2:p.Gly115Val
|
|
XM_011536675.1:c.344G>T
|
XP_011534977.1:p.Gly115Val
|
|
XM_011536676.1:c.11G>T
|
XP_011534978.1:p.Gly4Val
|
|
XM_011536677.1:c.344G>T
|
XP_011534979.1:p.Gly115Val
|
|
XM_011536678.1:c.344G>T
|
XP_011534980.1:p.Gly115Val
|
|
XM_011536680.1:c.344G>T
|
XP_011534982.1:p.Gly115Val
|
|
XR_943416.1:n.547G>T
|
|
|
XM_011536675.2:c.344G>T
|
XP_011534977.1:p.Gly115Val
|
|
XM_011536676.2:c.11G>T
|
XP_011534978.1:p.Gly4Val
|
|
XM_011536677.3:c.344G>T
|
XP_011534979.1:p.Gly115Val
|
|
XR_001750279.1:n.544G>T
|
|
|
XR_001750282.1:n.548G>T
|
|
|
XR_943416.3:n.545G>T
|
|
|
NM_013382.6:c.344G>T
|
NP_037514.2:p.Gly115Val
|
|
NM_013382.7:c.344G>T
MANE Select
|
NP_037514.2:p.Gly115Val
|
|