ENST00000695651.1:n.920C>T
|
|
|
ENST00000695652.1:c.2449C>T
|
ENSP00000512083.1:p.Gln817Ter
|
|
ENST00000695653.1:c.481C>T
|
ENSP00000512084.1:p.Gln161Ter
|
|
ENST00000695654.1:c.1696C>T
|
ENSP00000512085.1:p.Gln566Ter
|
|
ENST00000695655.1:c.1513C>T
|
ENSP00000512086.1:n.1513C>T
|
|
ENST00000695692.1:n.1936C>T
|
|
|
ENST00000245907.11:c.2572C>T
MANE Select
|
ENSP00000245907.4:p.Gln858Ter
|
|
ENST00000245907.10:c.2572C>T
|
ENSP00000245907.4:p.Gln858Ter
|
|
ENST00000594005.1:n.53C>T
|
|
|
ENST00000602053.1:n.620C>T
|
|
|
NM_000064.3:c.2572C>T
|
NP_000055.2:p.Gln858Ter
|
|
NM_000064.4:c.2572C>T
MANE Select
|
NP_000055.2:p.Gln858Ter
|
|