ENST00000555134.2:n.966T>A
|
|
|
ENST00000556394.2:c.1582T>A
|
ENSP00000451967.2:p.Trp528Arg
|
|
ENST00000682247.1:c.2030T>A
|
ENSP00000507213.1:p.Val677Glu
|
|
ENST00000682395.1:n.2505T>A
|
|
|
ENST00000682459.1:n.1744T>A
|
|
|
ENST00000682467.1:c.1900T>A
|
ENSP00000508062.1:p.Trp634Arg
|
|
ENST00000682795.1:c.2188T>A
|
ENSP00000507574.1:p.Trp730Arg
|
|
ENST00000682895.1:n.1757T>A
|
|
|
ENST00000682955.1:n.1615T>A
|
|
|
ENST00000683188.1:c.2302T>A
|
|
|
ENST00000683380.1:n.1705T>A
|
|
|
ENST00000683907.1:c.306T>A
|
ENSP00000507754.1:n.306T>A
|
|
ENST00000684259.1:n.3808T>A
|
|
|
ENST00000684538.1:n.1420T>A
|
|
|
ENST00000684549.1:n.1592T>A
|
|
|
ENST00000261534.9:c.2041T>A
MANE Select
|
ENSP00000261534.4:p.Trp681Arg
|
|
ENST00000261534.8:c.2041T>A
|
ENSP00000261534.4:p.Trp681Arg
|
|
ENST00000452340.7:n.3017T>A
|
|
|
ENST00000554767.5:n.2827T>A
|
|
|
ENST00000555710.1:c.402T>A
|
ENSP00000451730.1:n.402T>A
|
|
ENST00000556394.1:c.96T>A
|
|
|
ENST00000556446.1:n.342T>A
|
|
|
ENST00000602717.5:c.256T>A
|
ENSP00000487704.1:p.Trp86Arg
|
|
NM_013382.5:c.2041T>A , LRG_844t1:c.2041T>A
|
NP_037514.2:p.Trp681Arg
|
|
XM_011536675.1:c.2230T>A
|
XP_011534977.1:p.Trp744Arg
|
|
XM_011536676.1:c.1897T>A
|
XP_011534978.1:p.Trp633Arg
|
|
XM_011536677.1:c.1771T>A
|
XP_011534979.1:p.Trp591Arg
|
|
XM_011536679.1:c.1324T>A
|
XP_011534981.1:p.Trp442Arg
|
|
XR_943416.1:n.2294T>A
|
|
|
XM_011536675.2:c.2230T>A
|
XP_011534977.1:p.Trp744Arg
|
|
XM_011536676.2:c.1897T>A
|
XP_011534978.1:p.Trp633Arg
|
|
XM_011536677.3:c.1771T>A
|
XP_011534979.1:p.Trp591Arg
|
|
XR_001750279.1:n.2327T>A
|
|
|
XR_001750282.1:n.2980T>A
|
|
|
XR_943416.3:n.2292T>A
|
|
|
NM_013382.6:c.2041T>A
|
NP_037514.2:p.Trp681Arg
|
|
NM_013382.7:c.2041T>A
MANE Select
|
NP_037514.2:p.Trp681Arg
|
|