ENST00000682565.1:c.10517C>T
|
ENSP00000507671.1:p.Ala3506Val
|
|
ENST00000682801.1:c.10517C>T
|
ENSP00000507862.1:p.Ala3506Val
|
|
ENST00000682859.1:c.10517C>T
|
ENSP00000508222.1:p.Ala3506Val
|
|
ENST00000683791.1:c.3603C>T
|
|
|
ENST00000684460.1:c.7798C>T
|
|
|
ENST00000684548.1:c.10517C>T
|
ENSP00000507421.1:p.Ala3506Val
|
|
ENST00000684590.1:c.4964C>T
|
ENSP00000507376.1:p.Ala1655Val
|
|
ENST00000684656.1:c.7843C>T
|
|
|
ENST00000613296.6:c.10898C>T
MANE Select
|
ENSP00000482968.1:p.Ala3633Val
|
|
ENST00000651057.1:c.1052C>T
|
ENSP00000498504.1:p.Ala351Val
|
|
ENST00000651434.1:c.2254C>T
|
|
|
ENST00000651750.1:c.286C>T
|
|
|
ENST00000652487.1:c.1995C>T
|
|
|
ENST00000423048.5:c.4389C>T
|
ENSP00000399833.1:n.4389C>T
|
|
ENST00000484298.5:c.10772C>T
|
ENSP00000478155.1:p.Ala3591Val
|
|
ENST00000613296.4:c.10898C>T
|
ENSP00000482968.1:p.Ala3633Val
|
|
ENST00000614410.4:c.10898C>T
|
ENSP00000479094.1:p.Ala3633Val
|
|
ENST00000620466.4:n.4701C>T
|
|
|
NM_015120.4:c.10901C>T , LRG_741t1:c.10901C>T
|
NP_055935.4:p.Ala3634Val
|
|
NM_001378454.1:c.10898C>T
MANE Select
|
NP_001365383.1:p.Ala3633Val
|
|