ENST00000695651.1:n.2107G>C
|
|
|
ENST00000695652.1:c.3636G>C
|
ENSP00000512083.1:p.Val1212=
|
|
ENST00000695653.1:c.1668G>C
|
ENSP00000512084.1:p.Val556=
|
|
ENST00000695654.1:c.2784G>C
|
ENSP00000512085.1:p.Val928=
|
|
ENST00000695655.1:c.2700G>C
|
ENSP00000512086.1:n.2700G>C
|
|
ENST00000695692.1:n.3123G>C
|
|
|
ENST00000245907.11:c.3759G>C
MANE Select
|
ENSP00000245907.4:p.Val1253=
|
|
ENST00000245907.10:c.3759G>C
|
ENSP00000245907.4:p.Val1253=
|
|
ENST00000596238.1:n.202G>C
|
|
|
ENST00000601008.1:c.241+571G>C
|
ENSP00000471384.1:n.241+571G>C
|
|
NM_000064.3:c.3759G>C
|
NP_000055.2:p.Val1253=
|
|
NM_000064.4:c.3759G>C
MANE Select
|
NP_000055.2:p.Val1253=
|
|