ENST00000295897.9:c.1152C>T
MANE Select
|
ENSP00000295897.4:p.Cys384=
|
|
ENST00000295897.8:c.1152C>T
|
ENSP00000295897.4:p.Cys384=
|
|
ENST00000401494.7:c.807C>T
|
ENSP00000384695.3:p.Cys269=
|
|
ENST00000415165.6:c.576C>T
|
ENSP00000401820.2:p.Cys192=
|
|
ENST00000476441.6:c.*431C>T
|
ENSP00000423727.1:n.*431C>T
|
|
ENST00000484992.1:n.472C>T
|
|
|
ENST00000503124.5:c.702C>T
|
ENSP00000421027.1:p.Cys234=
|
|
ENST00000504043.1:n.155C>T
|
|
|
ENST00000505649.5:n.838C>T
|
|
|
ENST00000509063.5:c.1152C>T
|
ENSP00000422784.1:p.Cys384=
|
|
ENST00000511370.1:c.685C>T
|
|
|
ENST00000621085.4:c.513C>T
|
ENSP00000483421.1:p.Cys171=
|
|
ENST00000621628.4:c.513C>T
|
ENSP00000480485.1:p.Cys171=
|
|
NM_000477.5:c.1152C>T
|
NP_000468.1:p.Cys384=
|
|
NM_000477.6:c.1152C>T
|
NP_000468.1:p.Cys384=
|
|
NM_000477.7:c.1152C>T
MANE Select
|
NP_000468.1:p.Cys384=
|
|