ENST00000695651.1:n.848C>T
|
|
|
ENST00000695652.1:c.2377C>T
|
ENSP00000512083.1:p.Arg793Trp
|
|
ENST00000695653.1:c.409C>T
|
ENSP00000512084.1:p.Arg137Trp
|
|
ENST00000695654.1:c.1624C>T
|
ENSP00000512085.1:p.Arg542Trp
|
|
ENST00000695655.1:c.1441C>T
|
ENSP00000512086.1:n.1441C>T
|
|
ENST00000695692.1:n.1864C>T
|
|
|
ENST00000245907.11:c.2500C>T
MANE Select
|
ENSP00000245907.4:p.Arg834Trp
|
|
ENST00000245907.10:c.2500C>T
|
ENSP00000245907.4:p.Arg834Trp
|
|
ENST00000602053.1:n.548C>T
|
|
|
NM_000064.3:c.2500C>T
|
NP_000055.2:p.Arg834Trp
|
|
NM_000064.4:c.2500C>T
MANE Select
|
NP_000055.2:p.Arg834Trp
|
|