ENST00000541899.3:c.*299C>T
(TOMT)
MANE Select
|
ENSP00000494667.1:n.*299C>T
|
|
ENST00000541899.2:c.*299C>T
(TOMT)
|
ENSP00000494667.1:n.*299C>T
|
|
ENST00000307198.11:c.*299C>T
(LRRC51)
|
ENSP00000305742.7:n.*299C>T
|
|
ENST00000419228.2:c.*586C>T
(LRRC51)
|
ENSP00000392233.2:n.*586C>T
|
|
ENST00000427369.6:c.*894C>T
(LRRC51)
|
ENSP00000409403.2:n.*894C>T
|
|
ENST00000435085.5:c.*299C>T
(LRRC51)
|
ENSP00000409789.1:n.*299C>T
|
|
ENST00000502597.2:c.63+864G>A
(ANAPC15)
|
ENSP00000441774.1:n.63+864G>A
|
|
ENST00000538117.5:c.*98+5G>A
(ANAPC15)
|
ENSP00000445212.1:n.*98+5G>A
|
|
ENST00000543050.5:c.318+864G>A
(ANAPC15)
|
ENSP00000437360.1:n.318+864G>A
|
|
ENST00000544409.5:c.*894C>T
(LRRC51)
|
ENSP00000440969.1:n.*894C>T
|
|
NM_001145308.4:c.*299C>T
(LRTOMT)
|
NP_001138780.1:n.*299C>T
|
|
NM_001145309.3:c.*299C>T
(LRTOMT)
|
NP_001138781.1:n.*299C>T
|
|
NM_001145310.3:c.*299C>T
(LRTOMT)
|
NP_001138782.1:n.*299C>T
|
|
XM_011544849.1:c.1400C>T
(LRTOMT)
|
XP_011543151.1:n.1400C>T
|
|
NM_001330321.1:c.318+864G>A
(ANAPC15)
|
NP_001317250.1:n.318+864G>A
|
|
XM_024448401.1:c.1400C>T
(LRTOMT)
|
XP_024304169.1:n.1400C>T
|
|
NM_001145308.5:c.*299C>T
(LRTOMT)
|
NP_001138780.1:n.*299C>T
|
|
NM_001145309.4:c.*299C>T
(LRTOMT)
|
NP_001138781.1:n.*299C>T
|
|
NM_001145310.4:c.*299C>T
(LRTOMT)
|
NP_001138782.1:n.*299C>T
|
|
NM_001330321.2:c.318+864G>A
(ANAPC15)
|
NP_001317250.1:n.318+864G>A
|
|
NM_001393427.1:c.318+864G>A
(ANAPC15)
|
NP_001380356.1:n.318+864G>A
|
|
NM_001393428.1:c.318+864G>A
(ANAPC15)
|
NP_001380357.1:n.318+864G>A
|
|
NM_001393429.1:c.318+864G>A
(ANAPC15)
|
NP_001380358.1:n.318+864G>A
|
|
NM_001393430.1:c.318+864G>A
(ANAPC15)
|
NP_001380359.1:n.318+864G>A
|
|
NM_001393431.1:c.318+864G>A
(ANAPC15)
|
NP_001380360.1:n.318+864G>A
|
|
NM_001393443.1:c.319-349G>A
(ANAPC15)
|
NP_001380372.1:n.319-349G>A
|
|
NM_001393444.1:c.319-349G>A
(ANAPC15)
|
NP_001380373.1:n.319-349G>A
|
|
NM_001393445.1:c.319-349G>A
(ANAPC15)
|
NP_001380374.1:n.319-349G>A
|
|
NM_001393459.1:c.63+864G>A
(ANAPC15)
|
NP_001380388.1:n.63+864G>A
|
|
NM_001393500.1:c.*299C>T
(TOMT)
|
NP_001380429.1:n.*299C>T
|
|
NR_171687.1:n.567+5G>A
(ANAPC15)
|
|
|
NM_001393500.2:c.*299C>T
(TOMT)
MANE Select
|
NP_001380429.1:n.*299C>T
|
|