ENST00000682565.1:c.11731C>T
|
ENSP00000507671.1:p.Gln3911Ter
|
|
ENST00000682801.1:c.11167-751C>T
|
ENSP00000507862.1:n.11167-751C>T
|
|
ENST00000682859.1:c.11731C>T
|
ENSP00000508222.1:p.Gln3911Ter
|
|
ENST00000683791.1:c.4817C>T
|
|
|
ENST00000684460.1:c.9012C>T
|
|
|
ENST00000684548.1:c.11731C>T
|
ENSP00000507421.1:p.Gln3911Ter
|
|
ENST00000684590.1:c.6178C>T
|
ENSP00000507376.1:p.Gln2060Ter
|
|
ENST00000684656.1:c.9196C>T
|
|
|
ENST00000613296.6:c.12112C>T
MANE Select
|
ENSP00000482968.1:p.Gln4038Ter
|
|
ENST00000651057.1:c.2266C>T
|
ENSP00000498504.1:p.Gln756Ter
|
|
ENST00000651434.1:c.3468C>T
|
|
|
ENST00000651750.1:c.1260+553C>T
|
|
|
ENST00000652487.1:c.3283C>T
|
|
|
ENST00000464408.3:n.287C>T
|
|
|
ENST00000484298.5:c.11986C>T
|
ENSP00000478155.1:p.Gln3996Ter
|
|
ENST00000613296.4:c.12112C>T
|
ENSP00000482968.1:p.Gln4038Ter
|
|
ENST00000620466.4:n.5915C>T
|
|
|
NM_015120.4:c.12115C>T , LRG_741t1:c.12115C>T
|
NP_055935.4:p.Gln4039Ter
|
|
NM_001378454.1:c.12112C>T
MANE Select
|
NP_001365383.1:p.Gln4038Ter
|
|