ENST00000541899.3:c.179G=
(TOMT)
MANE Select
|
ENSP00000494667.1:p.Gly60=
|
|
ENST00000541899.2:c.179G=
(TOMT)
|
ENSP00000494667.1:p.Gly60=
|
|
ENST00000643715.1:c.438-2475G=
(LRTOMT)
|
ENSP00000496019.1:n.438-2475G=
|
|
ENST00000646163.1:c.147G=
(LRTOMT)
|
ENSP00000494749.1:p.Arg49=
|
|
ENST00000307198.11:c.278G=
(LRRC51)
|
ENSP00000305742.7:p.Gly93=
|
|
ENST00000419228.2:c.158G=
(LRRC51)
|
ENSP00000392233.2:p.Gly53=
|
|
ENST00000427369.6:c.681G=
(LRRC51)
|
ENSP00000409403.2:p.Arg227=
|
|
ENST00000435085.5:c.278G=
(LRRC51)
|
ENSP00000409789.1:p.Gly93=
|
|
ENST00000439209.5:c.438-2475G=
(LRRC51)
|
ENSP00000395139.1:n.438-2475G=
|
|
ENST00000541899.1:n.336G=
(LRRC51)
|
|
|
ENST00000544409.5:c.561G=
(LRRC51)
|
ENSP00000440969.1:p.Arg187=
|
|
NM_001145308.4:c.278G=
(LRTOMT)
|
NP_001138780.1:p.Gly93=
|
|
NM_001145309.3:c.278G=
(LRTOMT)
|
NP_001138781.1:p.Gly93=
|
|
NM_001145310.3:c.158G=
(LRTOMT)
|
NP_001138782.1:p.Gly53=
|
|
XM_011544849.1:c.503G=
(LRTOMT)
|
XP_011543151.1:p.Gly168=
|
|
XM_024448401.1:c.503G=
(LRTOMT)
|
XP_024304169.1:p.Gly168=
|
|
NM_001145308.5:c.278G=
(LRTOMT)
|
NP_001138780.1:p.Gly93=
|
|
NM_001145309.4:c.278G=
(LRTOMT)
|
NP_001138781.1:p.Gly93=
|
|
NM_001145310.4:c.158G=
(LRTOMT)
|
NP_001138782.1:p.Gly53=
|
|
NM_001393500.1:c.179G=
(TOMT)
|
NP_001380429.1:p.Gly60=
|
|
NM_001393500.2:c.179G=
(TOMT)
MANE Select
|
NP_001380429.1:p.Gly60=
|
|