ENST00000295897.9:c.1141C>T
MANE Select
|
ENSP00000295897.4:p.Leu381=
|
|
ENST00000295897.8:c.1141C>T
|
ENSP00000295897.4:p.Leu381=
|
|
ENST00000401494.7:c.796C>T
|
ENSP00000384695.3:p.Leu266=
|
|
ENST00000415165.6:c.565C>T
|
ENSP00000401820.2:p.Leu189=
|
|
ENST00000476441.6:c.*420C>T
|
ENSP00000423727.1:n.*420C>T
|
|
ENST00000484992.1:n.461C>T
|
|
|
ENST00000503124.5:c.691C>T
|
ENSP00000421027.1:p.Leu231=
|
|
ENST00000504043.1:n.144C>T
|
|
|
ENST00000505649.5:n.827C>T
|
|
|
ENST00000509063.5:c.1141C>T
|
ENSP00000422784.1:p.Leu381=
|
|
ENST00000511370.1:c.674C>T
|
|
|
ENST00000621085.4:c.502C>T
|
ENSP00000483421.1:p.Leu168=
|
|
ENST00000621628.4:c.502C>T
|
ENSP00000480485.1:p.Leu168=
|
|
NM_000477.5:c.1141C>T
|
NP_000468.1:p.Leu381=
|
|
NM_000477.6:c.1141C>T
|
NP_000468.1:p.Leu381=
|
|
NM_000477.7:c.1141C>T
MANE Select
|
NP_000468.1:p.Leu381=
|
|