ENST00000682565.1:c.10108T>C
|
ENSP00000507671.1:p.Cys3370Arg
|
|
ENST00000682801.1:c.10108T>C
|
ENSP00000507862.1:p.Cys3370Arg
|
|
ENST00000682859.1:c.10108T>C
|
ENSP00000508222.1:p.Cys3370Arg
|
|
ENST00000683791.1:c.3194T>C
|
|
|
ENST00000684460.1:c.7389T>C
|
|
|
ENST00000684548.1:c.10108T>C
|
ENSP00000507421.1:p.Cys3370Arg
|
|
ENST00000684590.1:c.4555T>C
|
ENSP00000507376.1:p.Cys1519Arg
|
|
ENST00000684656.1:c.7434T>C
|
|
|
ENST00000613296.6:c.10489T>C
MANE Select
|
ENSP00000482968.1:p.Cys3497Arg
|
|
ENST00000651057.1:c.643T>C
|
ENSP00000498504.1:p.Cys215Arg
|
|
ENST00000651434.1:c.1845T>C
|
|
|
ENST00000652487.1:c.1586T>C
|
|
|
ENST00000423048.5:c.3980T>C
|
ENSP00000399833.1:n.3980T>C
|
|
ENST00000484298.5:c.10363T>C
|
ENSP00000478155.1:p.Cys3455Arg
|
|
ENST00000613296.4:c.10489T>C
|
ENSP00000482968.1:p.Cys3497Arg
|
|
ENST00000614410.4:c.10489T>C
|
ENSP00000479094.1:p.Cys3497Arg
|
|
ENST00000620466.4:n.4292T>C
|
|
|
NM_015120.4:c.10492T>C , LRG_741t1:c.10492T>C
|
NP_055935.4:p.Cys3498Arg
|
|
NM_001378454.1:c.10489T>C
MANE Select
|
NP_001365383.1:p.Cys3497Arg
|
|