NM_000732.6:c.457C>T
MANE Select
|
NP_000723.1:p.Arg153Ter
|
ENST00000300692.9:c.457C>T
MANE Select
|
ENSP00000300692.4:p.Arg153Ter
|
NM_000732.4:c.457C>T , LRG_37t1:c.457C>T
|
NP_000723.1:p.Arg153Ter
|
NM_001040651.1:c.325C>T
|
NP_001035741.1:p.Arg109Ter
|
NM_001040651.2:c.325C>T
|
NP_001035741.1:p.Arg109Ter
|
ENST00000300692.8:c.457C>T
|
ENSP00000300692.4:p.Arg153Ter
|
ENST00000392884.2:c.325C>T
|
ENSP00000376622.2:p.Arg109Ter
|
ENST00000526561.1:n.130C>T
|
|
ENST00000529594.5:c.238C>T
|
ENSP00000437335.1:p.Arg80Ter
|
ENST00000534687.5:c.338C>T
|
|
ENST00000695666.1:n.1224C>T
|
|
ENST00000695667.1:n.742C>T
|
|