ENST00000682565.1:c.11608T>C
|
ENSP00000507671.1:p.Trp3870Arg
|
|
ENST00000682801.1:c.11167-874T>C
|
ENSP00000507862.1:n.11167-874T>C
|
|
ENST00000682859.1:c.11608T>C
|
ENSP00000508222.1:p.Trp3870Arg
|
|
ENST00000683791.1:c.4694T>C
|
|
|
ENST00000684460.1:c.8889T>C
|
|
|
ENST00000684548.1:c.11608T>C
|
ENSP00000507421.1:p.Trp3870Arg
|
|
ENST00000684590.1:c.6055T>C
|
ENSP00000507376.1:p.Trp2019Arg
|
|
ENST00000684656.1:c.9073T>C
|
|
|
ENST00000613296.6:c.11989T>C
MANE Select
|
ENSP00000482968.1:p.Trp3997Arg
|
|
ENST00000651057.1:c.2143T>C
|
ENSP00000498504.1:p.Trp715Arg
|
|
ENST00000651434.1:c.3345T>C
|
|
|
ENST00000651750.1:c.1260+430T>C
|
|
|
ENST00000652487.1:c.3160T>C
|
|
|
ENST00000464408.3:n.164T>C
|
|
|
ENST00000484298.5:c.11863T>C
|
ENSP00000478155.1:p.Trp3955Arg
|
|
ENST00000613296.4:c.11989T>C
|
ENSP00000482968.1:p.Trp3997Arg
|
|
ENST00000620466.4:n.5792T>C
|
|
|
NM_015120.4:c.11992T>C , LRG_741t1:c.11992T>C
|
NP_055935.4:p.Trp3998Arg
|
|
NM_001378454.1:c.11989T>C
MANE Select
|
NP_001365383.1:p.Trp3997Arg
|
|