ENST00000307363.10:c.1792C>T
MANE Select
|
ENSP00000306920.4:p.Gln598Ter
|
|
ENST00000307363.9:c.1792C>T
|
ENSP00000306920.4:p.Gln598Ter
|
|
ENST00000307377.12:c.1399C>T
|
ENSP00000305920.8:p.Gln467Ter
|
|
ENST00000399402.7:c.1702C>T
|
ENSP00000382333.2:p.Gln568Ter
|
|
NM_000404.2:c.1792C>T
|
NP_000395.2:p.Gln598Ter
|
|
NM_000404.3:c.1792C>T
|
NP_000395.2:p.Gln598Ter
|
|
NM_001079811.1:c.1702C>T
|
NP_001073279.1:p.Gln568Ter
|
|
NM_001079811.2:c.1702C>T
|
NP_001073279.1:p.Gln568Ter
|
|
NM_001135602.1:c.1399C>T
|
NP_001129074.1:p.Gln467Ter
|
|
NM_001135602.2:c.1399C>T
|
NP_001129074.1:p.Gln467Ter
|
|
NM_001317040.1:c.1936C>T
|
NP_001303969.1:p.Gln646Ter
|
|
NM_000404.4:c.1792C>T
MANE Select
|
NP_000395.3:p.Gln598Ter
|
|
NM_001079811.3:c.1702C>T
|
NP_001073279.2:p.Gln568Ter
|
|
NM_001135602.3:c.1399C>T
|
NP_001129074.2:p.Gln467Ter
|
|
NM_001317040.2:c.1936C>T
|
NP_001303969.2:p.Gln646Ter
|
|
NM_001393580.1:c.1734+16769C>T
|
NP_001380509.1:n.1734+16769C>T
|
|