ENST00000339077.10:c.946T>C
MANE Select
|
ENSP00000343273.4:p.Trp316Arg
|
|
ENST00000339077.9:c.946T>C
|
ENSP00000343273.4:p.Trp316Arg
|
|
ENST00000409689.5:c.802T>C
|
ENSP00000386263.1:p.Trp268Arg
|
|
ENST00000521082.5:c.*954T>C
|
ENSP00000430351.1:n.*954T>C
|
|
NM_001031710.2:c.946T>C
|
NP_001026880.2:p.Trp316Arg
|
|
NM_018846.4:c.802T>C
|
NP_061334.4:p.Trp268Arg
|
|
NR_033328.1:n.1370T>C
|
|
|
XM_006715753.1:c.985T>C
|
XP_006715816.1:p.Trp329Arg
|
|
XM_006715754.1:c.919T>C
|
XP_006715817.1:p.Trp307Arg
|
|
XM_006715755.1:c.919T>C
|
XP_006715818.1:p.Trp307Arg
|
|
XM_006715756.1:c.841T>C
|
XP_006715819.1:p.Trp281Arg
|
|
XM_006715753.3:c.985T>C
|
XP_006715816.1:p.Trp329Arg
|
|
XM_006715754.3:c.919T>C
|
XP_006715817.1:p.Trp307Arg
|
|
XM_006715755.3:c.919T>C
|
XP_006715818.1:p.Trp307Arg
|
|
XM_006715756.3:c.841T>C
|
XP_006715819.1:p.Trp281Arg
|
|
XM_017012439.2:c.880T>C
|
XP_016867928.1:p.Trp294Arg
|
|
NM_001031710.3:c.946T>C
MANE Select
|
NP_001026880.2:p.Trp316Arg
|
|
NM_018846.5:c.802T>C
|
NP_061334.4:p.Trp268Arg
|
|
NR_033328.2:n.1319T>C
|
|
|