ENST00000295897.9:c.258T>C
MANE Select
|
ENSP00000295897.4:p.Cys86=
|
|
ENST00000295897.8:c.258T>C
|
ENSP00000295897.4:p.Cys86=
|
|
ENST00000401494.7:c.137+1576T>C
|
ENSP00000384695.3:n.137+1576T>C
|
|
ENST00000415165.6:c.137+1576T>C
|
ENSP00000401820.2:n.137+1576T>C
|
|
ENST00000441319.5:c.264T>C
|
ENSP00000392541.1:p.Cys88=
|
|
ENST00000476441.6:c.79+2343T>C
|
ENSP00000423727.1:n.79+2343T>C
|
|
ENST00000503124.5:c.20T>C
|
ENSP00000421027.1:p.Val7Ala
|
|
ENST00000509063.5:c.258T>C
|
ENSP00000422784.1:p.Cys86=
|
|
ENST00000510166.5:n.294T>C
|
|
|
ENST00000514786.1:n.227T>C
|
|
|
ENST00000515133.5:n.299T>C
|
|
|
ENST00000621085.4:c.258T>C
|
ENSP00000483421.1:p.Cys86=
|
|
ENST00000621628.4:c.258T>C
|
ENSP00000480485.1:p.Cys86=
|
|
NM_000477.5:c.258T>C
|
NP_000468.1:p.Cys86=
|
|
NM_000477.6:c.258T>C
|
NP_000468.1:p.Cys86=
|
|
NM_000477.7:c.258T>C
MANE Select
|
NP_000468.1:p.Cys86=
|
|