ENST00000555134.2:n.993T>C
|
|
|
ENST00000556394.2:c.1609T>C
|
ENSP00000451967.2:p.Trp537Arg
|
|
ENST00000682247.1:c.2057T>C
|
ENSP00000507213.1:p.Leu686Pro
|
|
ENST00000682395.1:n.2532T>C
|
|
|
ENST00000682459.1:n.1771T>C
|
|
|
ENST00000682467.1:c.1927T>C
|
ENSP00000508062.1:p.Trp643Arg
|
|
ENST00000682795.1:c.2215T>C
|
ENSP00000507574.1:p.Trp739Arg
|
|
ENST00000682895.1:n.1784T>C
|
|
|
ENST00000682955.1:n.1642T>C
|
|
|
ENST00000683188.1:c.2329T>C
|
|
|
ENST00000683380.1:n.1732T>C
|
|
|
ENST00000683907.1:c.333T>C
|
ENSP00000507754.1:n.333T>C
|
|
ENST00000684259.1:n.3835T>C
|
|
|
ENST00000684538.1:n.1447T>C
|
|
|
ENST00000684549.1:n.1619T>C
|
|
|
ENST00000261534.9:c.2068T>C
MANE Select
|
ENSP00000261534.4:p.Trp690Arg
|
|
ENST00000261534.8:c.2068T>C
|
ENSP00000261534.4:p.Trp690Arg
|
|
ENST00000452340.7:n.3044T>C
|
|
|
ENST00000554767.5:n.2854T>C
|
|
|
ENST00000555710.1:c.429T>C
|
ENSP00000451730.1:n.429T>C
|
|
ENST00000556394.1:c.123T>C
|
|
|
ENST00000556446.1:n.369T>C
|
|
|
ENST00000602717.5:c.283T>C
|
ENSP00000487704.1:p.Trp95Arg
|
|
NM_013382.5:c.2068T>C , LRG_844t1:c.2068T>C
|
NP_037514.2:p.Trp690Arg
|
|
XM_011536675.1:c.2257T>C
|
XP_011534977.1:p.Trp753Arg
|
|
XM_011536676.1:c.1924T>C
|
XP_011534978.1:p.Trp642Arg
|
|
XM_011536677.1:c.1798T>C
|
XP_011534979.1:p.Trp600Arg
|
|
XM_011536679.1:c.1351T>C
|
XP_011534981.1:p.Trp451Arg
|
|
XR_943416.1:n.2321T>C
|
|
|
XM_011536675.2:c.2257T>C
|
XP_011534977.1:p.Trp753Arg
|
|
XM_011536676.2:c.1924T>C
|
XP_011534978.1:p.Trp642Arg
|
|
XM_011536677.3:c.1798T>C
|
XP_011534979.1:p.Trp600Arg
|
|
XR_001750279.1:n.2354T>C
|
|
|
XR_001750282.1:n.3007T>C
|
|
|
XR_943416.3:n.2319T>C
|
|
|
NM_013382.6:c.2068T>C
|
NP_037514.2:p.Trp690Arg
|
|
NM_013382.7:c.2068T>C
MANE Select
|
NP_037514.2:p.Trp690Arg
|
|