ENST00000553863.6:c.110-1590G>A
|
ENSP00000508202.1:n.110-1590G>A
|
|
ENST00000556394.2:c.357+1853G>A
|
ENSP00000451967.2:n.357+1853G>A
|
|
ENST00000556880.6:n.676G>A
|
|
|
ENST00000682247.1:c.652G>A
|
ENSP00000507213.1:p.Asp218Asn
|
|
ENST00000682377.1:c.232G>A
|
ENSP00000507494.1:p.Asp78Asn
|
|
ENST00000682382.1:c.495+1853G>A
|
|
|
ENST00000682395.1:n.381G>A
|
|
|
ENST00000682459.1:n.316G>A
|
|
|
ENST00000682467.1:c.652G>A
|
ENSP00000508062.1:p.Asp218Asn
|
|
ENST00000682795.1:c.652G>A
|
ENSP00000507574.1:p.Asp218Asn
|
|
ENST00000682895.1:n.368G>A
|
|
|
ENST00000682955.1:n.211+1853G>A
|
|
|
ENST00000683188.1:c.342+1853G>A
|
|
|
ENST00000683300.1:c.109+1853G>A
|
ENSP00000507630.1:n.109+1853G>A
|
|
ENST00000683328.1:c.109+1853G>A
|
ENSP00000508096.1:n.109+1853G>A
|
|
ENST00000683380.1:n.316G>A
|
|
|
ENST00000683551.1:c.105G>A
|
|
|
ENST00000683828.1:c.521G>A
|
|
|
ENST00000684259.1:n.503G>A
|
|
|
ENST00000684549.1:n.367+1853G>A
|
|
|
ENST00000261534.9:c.652G>A
MANE Select
|
ENSP00000261534.4:p.Asp218Asn
|
|
ENST00000261534.8:c.652G>A
|
ENSP00000261534.4:p.Asp218Asn
|
|
ENST00000452340.7:n.675G>A
|
|
|
ENST00000553863.5:n.316G>A
|
|
|
ENST00000554948.1:c.379G>A
|
ENSP00000452060.1:p.Asp127Asn
|
|
ENST00000555675.5:n.368G>A
|
|
|
ENST00000556326.5:c.*318G>A
|
ENSP00000450630.1:n.*318G>A
|
|
ENST00000556880.5:n.676G>A
|
|
|
ENST00000557289.1:c.55+1853G>A
|
ENSP00000451115.1:n.55+1853G>A
|
|
NM_013382.5:c.652G>A , LRG_844t1:c.652G>A
|
NP_037514.2:p.Asp218Asn
|
|
XM_011536675.1:c.652G>A
|
XP_011534977.1:p.Asp218Asn
|
|
XM_011536676.1:c.319G>A
|
XP_011534978.1:p.Asp107Asn
|
|
XM_011536677.1:c.547+1853G>A
|
XP_011534979.1:n.547+1853G>A
|
|
XM_011536678.1:c.652G>A
|
XP_011534980.1:p.Asp218Asn
|
|
XM_011536679.1:c.-91+1853G>A
|
XP_011534981.1:n.-91+1853G>A
|
|
XM_011536680.1:c.652G>A
|
XP_011534982.1:p.Asp218Asn
|
|
XR_943416.1:n.855G>A
|
|
|
XM_011536675.2:c.652G>A
|
XP_011534977.1:p.Asp218Asn
|
|
XM_011536676.2:c.319G>A
|
XP_011534978.1:p.Asp107Asn
|
|
XM_011536677.3:c.547+1853G>A
|
XP_011534979.1:n.547+1853G>A
|
|
XR_001750279.1:n.852G>A
|
|
|
XR_001750282.1:n.856G>A
|
|
|
XR_943416.3:n.853G>A
|
|
|
NM_013382.6:c.652G>A
|
NP_037514.2:p.Asp218Asn
|
|
NM_013382.7:c.652G>A
MANE Select
|
NP_037514.2:p.Asp218Asn
|
|