ENST00000295897.9:c.1798G=
MANE Select
|
ENSP00000295897.4:p.Val600=
|
|
ENST00000295897.8:c.1798G=
|
ENSP00000295897.4:p.Val600=
|
|
ENST00000401494.7:c.1453G=
|
ENSP00000384695.3:p.Val485=
|
|
ENST00000415165.6:c.1222G=
|
ENSP00000401820.2:p.Val408=
|
|
ENST00000476441.6:c.*1077G=
|
ENSP00000423727.1:n.*1077G=
|
|
ENST00000495173.1:n.106G=
|
|
|
ENST00000503124.5:c.1348G=
|
ENSP00000421027.1:p.Val450=
|
|
ENST00000505649.5:n.1345G=
|
|
|
ENST00000508932.5:n.188G=
|
|
|
ENST00000509063.5:c.1785+627G=
|
ENSP00000422784.1:n.1785+627G=
|
|
ENST00000511370.1:c.1331G=
|
|
|
ENST00000621085.4:c.1159G=
|
ENSP00000483421.1:p.Val387=
|
|
ENST00000621628.4:c.1159G=
|
ENSP00000480485.1:p.Val387=
|
|
NM_000477.5:c.1798G=
|
NP_000468.1:p.Val600=
|
|
NM_000477.6:c.1798G=
|
NP_000468.1:p.Val600=
|
|
NM_000477.7:c.1798G=
MANE Select
|
NP_000468.1:p.Val600=
|
|