ENST00000682565.1:c.10301A>T
|
ENSP00000507671.1:p.Asp3434Val
|
|
ENST00000682801.1:c.10301A>T
|
ENSP00000507862.1:p.Asp3434Val
|
|
ENST00000682859.1:c.10301A>T
|
ENSP00000508222.1:p.Asp3434Val
|
|
ENST00000683791.1:c.3387A>T
|
|
|
ENST00000684460.1:c.7582A>T
|
|
|
ENST00000684548.1:c.10301A>T
|
ENSP00000507421.1:p.Asp3434Val
|
|
ENST00000684590.1:c.4748A>T
|
ENSP00000507376.1:p.Asp1583Val
|
|
ENST00000684656.1:c.7627A>T
|
|
|
ENST00000613296.6:c.10682A>T
MANE Select
|
ENSP00000482968.1:p.Asp3561Val
|
|
ENST00000651057.1:c.836A>T
|
ENSP00000498504.1:p.Asp279Val
|
|
ENST00000651434.1:c.2038A>T
|
|
|
ENST00000651750.1:c.70A>T
|
|
|
ENST00000652487.1:c.1779A>T
|
|
|
ENST00000423048.5:c.4173A>T
|
ENSP00000399833.1:n.4173A>T
|
|
ENST00000484298.5:c.10556A>T
|
ENSP00000478155.1:p.Asp3519Val
|
|
ENST00000613296.4:c.10682A>T
|
ENSP00000482968.1:p.Asp3561Val
|
|
ENST00000614410.4:c.10682A>T
|
ENSP00000479094.1:p.Asp3561Val
|
|
ENST00000620466.4:n.4485A>T
|
|
|
NM_015120.4:c.10685A>T , LRG_741t1:c.10685A>T
|
NP_055935.4:p.Asp3562Val
|
|
NM_001378454.1:c.10682A>T
MANE Select
|
NP_001365383.1:p.Asp3561Val
|
|