ENST00000295897.9:c.1800T>A
MANE Select
|
ENSP00000295897.4:p.Val600=
|
|
ENST00000295897.8:c.1800T>A
|
ENSP00000295897.4:p.Val600=
|
|
ENST00000401494.7:c.1455T>A
|
ENSP00000384695.3:p.Val485=
|
|
ENST00000415165.6:c.1224T>A
|
ENSP00000401820.2:p.Val408=
|
|
ENST00000476441.6:c.*1079T>A
|
ENSP00000423727.1:n.*1079T>A
|
|
ENST00000495173.1:n.108T>A
|
|
|
ENST00000503124.5:c.1350T>A
|
ENSP00000421027.1:p.Val450=
|
|
ENST00000505649.5:n.1347T>A
|
|
|
ENST00000508932.5:n.190T>A
|
|
|
ENST00000509063.5:c.1785+629T>A
|
ENSP00000422784.1:n.1785+629T>A
|
|
ENST00000511370.1:c.1333T>A
|
|
|
ENST00000621085.4:c.1161T>A
|
ENSP00000483421.1:p.Val387=
|
|
ENST00000621628.4:c.1161T>A
|
ENSP00000480485.1:p.Val387=
|
|
NM_000477.5:c.1800T>A
|
NP_000468.1:p.Val600=
|
|
NM_000477.6:c.1800T>A
|
NP_000468.1:p.Val600=
|
|
NM_000477.7:c.1800T>A
MANE Select
|
NP_000468.1:p.Val600=
|
|