ENST00000541899.3:c.168T>C
(TOMT)
MANE Select
|
ENSP00000494667.1:p.His56=
|
|
ENST00000541899.2:c.168T>C
(TOMT)
|
ENSP00000494667.1:p.His56=
|
|
ENST00000643715.1:c.438-2486T>C
(LRTOMT)
|
ENSP00000496019.1:n.438-2486T>C
|
|
ENST00000646163.1:c.136T>C
(LRTOMT)
|
ENSP00000494749.1:p.Cys46Arg
|
|
ENST00000307198.11:c.267T>C
(LRRC51)
|
ENSP00000305742.7:p.His89=
|
|
ENST00000419228.2:c.147T>C
(LRRC51)
|
ENSP00000392233.2:p.His49=
|
|
ENST00000427369.6:c.670T>C
(LRRC51)
|
ENSP00000409403.2:p.Cys224Arg
|
|
ENST00000435085.5:c.267T>C
(LRRC51)
|
ENSP00000409789.1:p.His89=
|
|
ENST00000439209.5:c.438-2486T>C
(LRRC51)
|
ENSP00000395139.1:n.438-2486T>C
|
|
ENST00000541899.1:n.325T>C
(LRRC51)
|
|
|
ENST00000544409.5:c.550T>C
(LRRC51)
|
ENSP00000440969.1:p.Cys184Arg
|
|
NM_001145308.4:c.267T>C
(LRTOMT)
|
NP_001138780.1:p.His89=
|
|
NM_001145309.3:c.267T>C
(LRTOMT)
|
NP_001138781.1:p.His89=
|
|
NM_001145310.3:c.147T>C
(LRTOMT)
|
NP_001138782.1:p.His49=
|
|
XM_011544849.1:c.492T>C
(LRTOMT)
|
XP_011543151.1:p.His164=
|
|
XM_024448401.1:c.492T>C
(LRTOMT)
|
XP_024304169.1:p.His164=
|
|
NM_001145308.5:c.267T>C
(LRTOMT)
|
NP_001138780.1:p.His89=
|
|
NM_001145309.4:c.267T>C
(LRTOMT)
|
NP_001138781.1:p.His89=
|
|
NM_001145310.4:c.147T>C
(LRTOMT)
|
NP_001138782.1:p.His49=
|
|
NM_001393500.1:c.168T>C
(TOMT)
|
NP_001380429.1:p.His56=
|
|
NM_001393500.2:c.168T>C
(TOMT)
MANE Select
|
NP_001380429.1:p.His56=
|
|