ENST00000541899.3:c.168T>G
(TOMT)
MANE Select
|
ENSP00000494667.1:p.His56Gln
|
|
ENST00000541899.2:c.168T>G
(TOMT)
|
ENSP00000494667.1:p.His56Gln
|
|
ENST00000643715.1:c.438-2486T>G
(LRTOMT)
|
ENSP00000496019.1:n.438-2486T>G
|
|
ENST00000646163.1:c.136T>G
(LRTOMT)
|
ENSP00000494749.1:p.Cys46Gly
|
|
ENST00000307198.11:c.267T>G
(LRRC51)
|
ENSP00000305742.7:p.His89Gln
|
|
ENST00000419228.2:c.147T>G
(LRRC51)
|
ENSP00000392233.2:p.His49Gln
|
|
ENST00000427369.6:c.670T>G
(LRRC51)
|
ENSP00000409403.2:p.Cys224Gly
|
|
ENST00000435085.5:c.267T>G
(LRRC51)
|
ENSP00000409789.1:p.His89Gln
|
|
ENST00000439209.5:c.438-2486T>G
(LRRC51)
|
ENSP00000395139.1:n.438-2486T>G
|
|
ENST00000541899.1:n.325T>G
(LRRC51)
|
|
|
ENST00000544409.5:c.550T>G
(LRRC51)
|
ENSP00000440969.1:p.Cys184Gly
|
|
NM_001145308.4:c.267T>G
(LRTOMT)
|
NP_001138780.1:p.His89Gln
|
|
NM_001145309.3:c.267T>G
(LRTOMT)
|
NP_001138781.1:p.His89Gln
|
|
NM_001145310.3:c.147T>G
(LRTOMT)
|
NP_001138782.1:p.His49Gln
|
|
XM_011544849.1:c.492T>G
(LRTOMT)
|
XP_011543151.1:p.His164Gln
|
|
XM_024448401.1:c.492T>G
(LRTOMT)
|
XP_024304169.1:p.His164Gln
|
|
NM_001145308.5:c.267T>G
(LRTOMT)
|
NP_001138780.1:p.His89Gln
|
|
NM_001145309.4:c.267T>G
(LRTOMT)
|
NP_001138781.1:p.His89Gln
|
|
NM_001145310.4:c.147T>G
(LRTOMT)
|
NP_001138782.1:p.His49Gln
|
|
NM_001393500.1:c.168T>G
(TOMT)
|
NP_001380429.1:p.His56Gln
|
|
NM_001393500.2:c.168T>G
(TOMT)
MANE Select
|
NP_001380429.1:p.His56Gln
|
|