|
ENST00000555134.2:n.1167T>C
|
|
|
|
ENST00000556394.2:c.1783T>C
|
ENSP00000451967.2:p.Trp595Arg
|
|
|
ENST00000682247.1:c.2231T>C
|
ENSP00000507213.1:p.Met744Thr
|
|
|
ENST00000682395.1:n.2706T>C
|
|
|
|
ENST00000682459.1:n.1945T>C
|
|
|
|
ENST00000682467.1:c.2101T>C
|
ENSP00000508062.1:p.Trp701Arg
|
|
|
ENST00000682795.1:c.2389T>C
|
ENSP00000507574.1:p.Trp797Arg
|
|
|
ENST00000682895.1:n.1958T>C
|
|
|
|
ENST00000682897.1:c.95T>C
|
|
|
|
ENST00000682955.1:n.1816T>C
|
|
|
|
ENST00000683188.1:c.2503T>C
|
|
|
|
ENST00000683380.1:n.1906T>C
|
|
|
|
ENST00000683784.1:c.95T>C
|
|
|
|
ENST00000684259.1:n.4009T>C
|
|
|
|
ENST00000684538.1:n.1621T>C
|
|
|
|
ENST00000684549.1:n.1793T>C
|
|
|
|
ENST00000261534.9:c.2242T>C
MANE Select
|
ENSP00000261534.4:p.Trp748Arg
|
|
|
ENST00000261534.8:c.2242T>C
|
ENSP00000261534.4:p.Trp748Arg
|
|
|
ENST00000452340.7:n.3218T>C
|
|
|
|
ENST00000554767.5:n.3028T>C
|
|
|
|
ENST00000556394.1:c.297T>C
|
|
|
|
ENST00000602717.5:c.363-109T>C
|
ENSP00000487704.1:n.363-109T>C
|
|
|
NM_013382.5:c.2242T>C , LRG_844t1:c.2242T>C
|
NP_037514.2:p.Trp748Arg
|
|
|
XM_011536675.1:c.2431T>C
|
XP_011534977.1:p.Trp811Arg
|
|
|
XM_011536676.1:c.2098T>C
|
XP_011534978.1:p.Trp700Arg
|
|
|
XM_011536677.1:c.1972T>C
|
XP_011534979.1:p.Trp658Arg
|
|
|
XM_011536679.1:c.1525T>C
|
XP_011534981.1:p.Trp509Arg
|
|
|
XR_943416.1:n.2495T>C
|
|
|
|
XM_011536675.2:c.2431T>C
|
XP_011534977.1:p.Trp811Arg
|
|
|
XM_011536676.2:c.2098T>C
|
XP_011534978.1:p.Trp700Arg
|
|
|
XM_011536677.3:c.1972T>C
|
XP_011534979.1:p.Trp658Arg
|
|
|
XR_001750279.1:n.2528T>C
|
|
|
|
XR_001750282.1:n.3181T>C
|
|
|
|
XR_943416.3:n.2493T>C
|
|
|
|
NM_013382.6:c.2242T>C
|
NP_037514.2:p.Trp748Arg
|
|
|
NM_013382.7:c.2242T>C
MANE Select
|
NP_037514.2:p.Trp748Arg
|
|
