ENST00000682565.1:c.7582C>T
|
ENSP00000507671.1:p.Gln2528Ter
|
|
ENST00000682801.1:c.7582C>T
|
ENSP00000507862.1:p.Gln2528Ter
|
|
ENST00000682859.1:c.7582C>T
|
ENSP00000508222.1:p.Gln2528Ter
|
|
ENST00000683791.1:c.974C>T
|
|
|
ENST00000684460.1:c.5034C>T
|
|
|
ENST00000684548.1:c.7582C>T
|
ENSP00000507421.1:p.Gln2528Ter
|
|
ENST00000684590.1:c.2029C>T
|
ENSP00000507376.1:p.Gln677Ter
|
|
ENST00000684656.1:c.5034C>T
|
|
|
ENST00000613296.6:c.7963C>T
MANE Select
|
ENSP00000482968.1:p.Gln2655Ter
|
|
ENST00000651434.1:c.896-29853C>T
|
|
|
ENST00000423048.5:c.2794C>T
|
ENSP00000399833.1:p.Gln932Ter
|
|
ENST00000484298.5:c.7837C>T
|
ENSP00000478155.1:p.Gln2613Ter
|
|
ENST00000613296.4:c.7963C>T
|
ENSP00000482968.1:p.Gln2655Ter
|
|
ENST00000614410.4:c.7963C>T
|
ENSP00000479094.1:p.Gln2655Ter
|
|
ENST00000620466.4:n.1766C>T
|
|
|
NM_015120.4:c.7966C>T , LRG_741t1:c.7966C>T
|
NP_055935.4:p.Gln2656Ter
|
|
NM_001378454.1:c.7963C>T
MANE Select
|
NP_001365383.1:p.Gln2655Ter
|
|