ENST00000695651.1:n.1079G>T
|
|
|
ENST00000695652.1:c.2608G>T
|
ENSP00000512083.1:p.Glu870Ter
|
|
ENST00000695653.1:c.640G>T
|
ENSP00000512084.1:p.Glu214Ter
|
|
ENST00000695654.1:c.1855G>T
|
ENSP00000512085.1:p.Glu619Ter
|
|
ENST00000695655.1:c.1672G>T
|
ENSP00000512086.1:n.1672G>T
|
|
ENST00000695692.1:n.2095G>T
|
|
|
ENST00000245907.11:c.2731G>T
MANE Select
|
ENSP00000245907.4:p.Glu911Ter
|
|
ENST00000245907.10:c.2731G>T
|
ENSP00000245907.4:p.Glu911Ter
|
|
ENST00000594005.1:n.307G>T
|
|
|
NM_000064.3:c.2731G>T
|
NP_000055.2:p.Glu911Ter
|
|
NM_000064.4:c.2731G>T
MANE Select
|
NP_000055.2:p.Glu911Ter
|
|