ENST00000295897.9:c.259G=
MANE Select
|
ENSP00000295897.4:p.Asp87=
|
|
ENST00000295897.8:c.259G=
|
ENSP00000295897.4:p.Asp87=
|
|
ENST00000401494.7:c.137+1577G=
|
ENSP00000384695.3:n.137+1577G=
|
|
ENST00000415165.6:c.137+1577G=
|
ENSP00000401820.2:n.137+1577G=
|
|
ENST00000441319.5:c.265G=
|
ENSP00000392541.1:p.Asp89=
|
|
ENST00000476441.6:c.79+2344G=
|
ENSP00000423727.1:n.79+2344G=
|
|
ENST00000503124.5:c.21G=
|
ENSP00000421027.1:p.Val7=
|
|
ENST00000509063.5:c.259G=
|
ENSP00000422784.1:p.Asp87=
|
|
ENST00000510166.5:n.295G=
|
|
|
ENST00000514786.1:n.228G=
|
|
|
ENST00000515133.5:n.300G=
|
|
|
ENST00000621085.4:c.259G=
|
ENSP00000483421.1:p.Asp87=
|
|
ENST00000621628.4:c.259G=
|
ENSP00000480485.1:p.Asp87=
|
|
NM_000477.5:c.259G=
|
NP_000468.1:p.Asp87=
|
|
NM_000477.6:c.259G=
|
NP_000468.1:p.Asp87=
|
|
NM_000477.7:c.259G=
MANE Select
|
NP_000468.1:p.Asp87=
|
|