ENST00000541899.3:c.633T>C
(TOMT)
MANE Select
|
ENSP00000494667.1:p.His211=
|
|
ENST00000541899.2:c.633T>C
(TOMT)
|
ENSP00000494667.1:p.His211=
|
|
ENST00000643715.1:c.*143T>C
(LRTOMT)
|
ENSP00000496019.1:n.*143T>C
|
|
ENST00000307198.11:c.732T>C
(LRRC51)
|
ENSP00000305742.7:p.His244=
|
|
ENST00000419228.2:c.*143T>C
(LRRC51)
|
ENSP00000392233.2:n.*143T>C
|
|
ENST00000427369.6:c.*451T>C
(LRRC51)
|
ENSP00000409403.2:n.*451T>C
|
|
ENST00000435085.5:c.732T>C
(LRRC51)
|
ENSP00000409789.1:p.His244=
|
|
ENST00000439209.5:c.*143T>C
(LRRC51)
|
ENSP00000395139.1:n.*143T>C
|
|
ENST00000502597.2:c.64-1176A>G
(ANAPC15)
|
ENSP00000441774.1:n.64-1176A>G
|
|
ENST00000543050.5:c.319-1176A>G
(ANAPC15)
|
ENSP00000437360.1:n.319-1176A>G
|
|
ENST00000544409.5:c.*451T>C
(LRRC51)
|
ENSP00000440969.1:n.*451T>C
|
|
NM_001145308.4:c.732T>C
(LRTOMT)
|
NP_001138780.1:p.His244=
|
|
NM_001145309.3:c.732T>C
(LRTOMT)
|
NP_001138781.1:p.His244=
|
|
NM_001145310.3:c.612T>C
(LRTOMT)
|
NP_001138782.1:p.His204=
|
|
XM_011544849.1:c.957T>C
(LRTOMT)
|
XP_011543151.1:p.His319=
|
|
NM_001330321.1:c.319-1176A>G
(ANAPC15)
|
NP_001317250.1:n.319-1176A>G
|
|
XM_024448401.1:c.957T>C
(LRTOMT)
|
XP_024304169.1:p.His319=
|
|
NM_001145308.5:c.732T>C
(LRTOMT)
|
NP_001138780.1:p.His244=
|
|
NM_001145309.4:c.732T>C
(LRTOMT)
|
NP_001138781.1:p.His244=
|
|
NM_001145310.4:c.612T>C
(LRTOMT)
|
NP_001138782.1:p.His204=
|
|
NM_001330321.2:c.319-1176A>G
(ANAPC15)
|
NP_001317250.1:n.319-1176A>G
|
|
NM_001393427.1:c.319-1176A>G
(ANAPC15)
|
NP_001380356.1:n.319-1176A>G
|
|
NM_001393428.1:c.319-1176A>G
(ANAPC15)
|
NP_001380357.1:n.319-1176A>G
|
|
NM_001393429.1:c.319-1176A>G
(ANAPC15)
|
NP_001380358.1:n.319-1176A>G
|
|
NM_001393430.1:c.319-1176A>G
(ANAPC15)
|
NP_001380359.1:n.319-1176A>G
|
|
NM_001393431.1:c.319-1176A>G
(ANAPC15)
|
NP_001380360.1:n.319-1176A>G
|
|
NM_001393443.1:c.*38A>G
(ANAPC15)
|
NP_001380372.1:n.*38A>G
|
|
NM_001393444.1:c.*38A>G
(ANAPC15)
|
NP_001380373.1:n.*38A>G
|
|
NM_001393445.1:c.*38A>G
(ANAPC15)
|
NP_001380374.1:n.*38A>G
|
|
NM_001393459.1:c.64-1176A>G
(ANAPC15)
|
NP_001380388.1:n.64-1176A>G
|
|
NM_001393500.1:c.633T>C
(TOMT)
|
NP_001380429.1:p.His211=
|
|
NR_171687.1:n.662A>G
(ANAPC15)
|
|
|
NM_001393500.2:c.633T>C
(TOMT)
MANE Select
|
NP_001380429.1:p.His211=
|
|