ENST00000541899.3:c.125G>T
(TOMT)
MANE Select
|
ENSP00000494667.1:p.Gly42Val
|
|
ENST00000541899.2:c.125G>T
(TOMT)
|
ENSP00000494667.1:p.Gly42Val
|
|
ENST00000643715.1:c.438-2529G>T
(LRTOMT)
|
ENSP00000496019.1:n.438-2529G>T
|
|
ENST00000646163.1:c.93G>T
(LRTOMT)
|
ENSP00000494749.1:p.Arg31Ser
|
|
ENST00000307198.11:c.224G>T
(LRRC51)
|
ENSP00000305742.7:p.Gly75Val
|
|
ENST00000419228.2:c.104G>T
(LRRC51)
|
ENSP00000392233.2:p.Gly35Val
|
|
ENST00000427369.6:c.627G>T
(LRRC51)
|
ENSP00000409403.2:p.Arg209Ser
|
|
ENST00000435085.5:c.224G>T
(LRRC51)
|
ENSP00000409789.1:p.Gly75Val
|
|
ENST00000439209.5:c.438-2529G>T
(LRRC51)
|
ENSP00000395139.1:n.438-2529G>T
|
|
ENST00000541899.1:n.282G>T
(LRRC51)
|
|
|
ENST00000544409.5:c.507G>T
(LRRC51)
|
ENSP00000440969.1:p.Arg169Ser
|
|
NM_001145308.4:c.224G>T
(LRTOMT)
|
NP_001138780.1:p.Gly75Val
|
|
NM_001145309.3:c.224G>T
(LRTOMT)
|
NP_001138781.1:p.Gly75Val
|
|
NM_001145310.3:c.104G>T
(LRTOMT)
|
NP_001138782.1:p.Gly35Val
|
|
XM_011544849.1:c.449G>T
(LRTOMT)
|
XP_011543151.1:p.Gly150Val
|
|
XM_024448401.1:c.449G>T
(LRTOMT)
|
XP_024304169.1:p.Gly150Val
|
|
NM_001145308.5:c.224G>T
(LRTOMT)
|
NP_001138780.1:p.Gly75Val
|
|
NM_001145309.4:c.224G>T
(LRTOMT)
|
NP_001138781.1:p.Gly75Val
|
|
NM_001145310.4:c.104G>T
(LRTOMT)
|
NP_001138782.1:p.Gly35Val
|
|
NM_001393500.1:c.125G>T
(TOMT)
|
NP_001380429.1:p.Gly42Val
|
|
NM_001393500.2:c.125G>T
(TOMT)
MANE Select
|
NP_001380429.1:p.Gly42Val
|
|