ENST00000695651.1:n.1111C>T
|
|
|
ENST00000695652.1:c.2640C>T
|
ENSP00000512083.1:p.Ile880=
|
|
ENST00000695653.1:c.672C>T
|
ENSP00000512084.1:p.Ile224=
|
|
ENST00000695654.1:c.1887C>T
|
ENSP00000512085.1:p.Ile629=
|
|
ENST00000695655.1:c.1704C>T
|
ENSP00000512086.1:n.1704C>T
|
|
ENST00000695692.1:n.2127C>T
|
|
|
ENST00000245907.11:c.2763C>T
MANE Select
|
ENSP00000245907.4:p.Ile921=
|
|
ENST00000245907.10:c.2763C>T
|
ENSP00000245907.4:p.Ile921=
|
|
ENST00000594005.1:n.339C>T
|
|
|
NM_000064.3:c.2763C>T
|
NP_000055.2:p.Ile921=
|
|
NM_000064.4:c.2763C>T
MANE Select
|
NP_000055.2:p.Ile921=
|
|