ENST00000682565.1:c.10384G>T
|
ENSP00000507671.1:p.Glu3462Ter
|
|
ENST00000682801.1:c.10384G>T
|
ENSP00000507862.1:p.Glu3462Ter
|
|
ENST00000682859.1:c.10384G>T
|
ENSP00000508222.1:p.Glu3462Ter
|
|
ENST00000683791.1:c.3470G>T
|
|
|
ENST00000684460.1:c.7665G>T
|
|
|
ENST00000684548.1:c.10384G>T
|
ENSP00000507421.1:p.Glu3462Ter
|
|
ENST00000684590.1:c.4831G>T
|
ENSP00000507376.1:p.Glu1611Ter
|
|
ENST00000684656.1:c.7710G>T
|
|
|
ENST00000613296.6:c.10765G>T
MANE Select
|
ENSP00000482968.1:p.Glu3589Ter
|
|
ENST00000651057.1:c.919G>T
|
ENSP00000498504.1:p.Glu307Ter
|
|
ENST00000651434.1:c.2121G>T
|
|
|
ENST00000651750.1:c.153G>T
|
|
|
ENST00000652487.1:c.1862G>T
|
|
|
ENST00000423048.5:c.4256G>T
|
ENSP00000399833.1:n.4256G>T
|
|
ENST00000484298.5:c.10639G>T
|
ENSP00000478155.1:p.Glu3547Ter
|
|
ENST00000613296.4:c.10765G>T
|
ENSP00000482968.1:p.Glu3589Ter
|
|
ENST00000614410.4:c.10765G>T
|
ENSP00000479094.1:p.Glu3589Ter
|
|
ENST00000620466.4:n.4568G>T
|
|
|
NM_015120.4:c.10768G>T , LRG_741t1:c.10768G>T
|
NP_055935.4:p.Glu3590Ter
|
|
NM_001378454.1:c.10765G>T
MANE Select
|
NP_001365383.1:p.Glu3589Ter
|
|