ENST00000541899.3:c.12C>G
(TOMT)
MANE Select
|
ENSP00000494667.1:p.Ala4=
|
|
ENST00000541899.2:c.12C>G
(TOMT)
|
ENSP00000494667.1:p.Ala4=
|
|
ENST00000643715.1:c.438-2642C>G
(LRTOMT)
|
ENSP00000496019.1:n.438-2642C>G
|
|
ENST00000646163.1:c.73-93C>G
(LRTOMT)
|
ENSP00000494749.1:n.73-93C>G
|
|
ENST00000307198.11:c.111C>G
(LRRC51)
|
ENSP00000305742.7:p.Ala37=
|
|
ENST00000419228.2:c.84-93C>G
(LRRC51)
|
ENSP00000392233.2:n.84-93C>G
|
|
ENST00000427369.6:c.514C>G
(LRRC51)
|
ENSP00000409403.2:p.His172Asp
|
|
ENST00000435085.5:c.111C>G
(LRRC51)
|
ENSP00000409789.1:p.Ala37=
|
|
ENST00000439209.5:c.438-2642C>G
(LRRC51)
|
ENSP00000395139.1:n.438-2642C>G
|
|
ENST00000541899.1:n.169C>G
(LRRC51)
|
|
|
ENST00000544409.5:c.487-93C>G
(LRRC51)
|
ENSP00000440969.1:n.487-93C>G
|
|
NM_001145308.4:c.111C>G
(LRTOMT)
|
NP_001138780.1:p.Ala37=
|
|
NM_001145309.3:c.111C>G
(LRTOMT)
|
NP_001138781.1:p.Ala37=
|
|
NM_001145310.3:c.84-93C>G
(LRTOMT)
|
NP_001138782.1:n.84-93C>G
|
|
XM_011544849.1:c.336C>G
(LRTOMT)
|
XP_011543151.1:p.Ala112=
|
|
XM_024448401.1:c.336C>G
(LRTOMT)
|
XP_024304169.1:p.Ala112=
|
|
NM_001145308.5:c.111C>G
(LRTOMT)
|
NP_001138780.1:p.Ala37=
|
|
NM_001145309.4:c.111C>G
(LRTOMT)
|
NP_001138781.1:p.Ala37=
|
|
NM_001145310.4:c.84-93C>G
(LRTOMT)
|
NP_001138782.1:n.84-93C>G
|
|
NM_001393500.1:c.12C>G
(TOMT)
|
NP_001380429.1:p.Ala4=
|
|
NM_001393500.2:c.12C>G
(TOMT)
MANE Select
|
NP_001380429.1:p.Ala4=
|
|