ENST00000396373.9:c.1240A>T
MANE Select
|
ENSP00000379658.3:p.Arg414Trp
|
|
ENST00000266427.3:c.77A>T
|
|
|
ENST00000396373.8:c.1240A>T
|
ENSP00000379658.3:p.Arg414Trp
|
|
NM_001987.4:c.1240A>T , LRG_609t1:c.1240A>T
|
NP_001978.1:p.Arg414Trp
|
|
XM_011520607.1:c.1237A>T
|
XP_011518909.1:p.Arg413Trp
|
|
XM_011520608.1:c.1213A>T
|
XP_011518910.1:p.Arg405Trp
|
|
XM_011520609.1:c.976A>T
|
XP_011518911.1:p.Arg326Trp
|
|
XM_011520610.1:c.976A>T
|
XP_011518912.1:p.Arg326Trp
|
|
XM_011520611.1:c.976A>T
|
XP_011518913.1:p.Arg326Trp
|
|
XM_011520612.1:c.619A>T
|
XP_011518914.1:p.Arg207Trp
|
|
XM_011520607.2:c.1237A>T
|
XP_011518909.1:p.Arg413Trp
|
|
XM_011520608.2:c.1213A>T
|
XP_011518910.1:p.Arg405Trp
|
|
XM_011520609.2:c.976A>T
|
XP_011518911.1:p.Arg326Trp
|
|
XM_011520611.2:c.976A>T
|
XP_011518913.1:p.Arg326Trp
|
|
XM_011520612.2:c.619A>T
|
XP_011518914.1:p.Arg207Trp
|
|
XM_017018990.1:c.1105A>T
|
XP_016874479.1:p.Arg369Trp
|
|
XM_017018991.1:c.976A>T
|
XP_016874480.1:p.Arg326Trp
|
|
NM_001987.5:c.1240A>T
MANE Select
|
NP_001978.1:p.Arg414Trp
|
|