ENST00000295497.13:c.297C>T
|
ENSP00000295497.7:p.Asn99=
|
|
ENST00000444394.7:c.297C>T
|
ENSP00000411911.2:p.Asn99=
|
|
ENST00000295497.12:c.297C>T
|
ENSP00000295497.7:p.Asn99=
|
|
ENST00000409089.7:c.-4C>T
|
ENSP00000386322.3:n.-4C>T
|
|
ENST00000409900.9:c.672C>T
MANE Select
|
ENSP00000386741.4:p.Asn224=
|
|
ENST00000413882.6:c.126C>T
|
ENSP00000410496.2:p.Asn42=
|
|
ENST00000425395.6:c.*119C>T
|
ENSP00000405270.2:n.*119C>T
|
|
ENST00000443238.6:c.150C>T
|
ENSP00000409798.2:p.Asn50=
|
|
ENST00000444394.6:c.297C>T
|
ENSP00000411911.2:p.Asn99=
|
|
ENST00000444573.2:c.516C>T
|
ENSP00000392603.2:p.Asn172=
|
|
ENST00000488080.6:n.315C>T
|
|
|
ENST00000650731.1:c.-4C>T
|
ENSP00000499146.1:n.-4C>T
|
|
ENST00000650938.1:c.196C>T
|
|
|
ENST00000651246.1:c.264C>T
|
ENSP00000498484.1:p.Asn88=
|
|
ENST00000651373.1:c.186C>T
|
ENSP00000499174.1:p.Asn62=
|
|
ENST00000651501.1:c.*119C>T
|
ENSP00000498894.1:n.*119C>T
|
|
ENST00000651717.1:c.253-11992C>T
|
ENSP00000499124.1:n.253-11992C>T
|
|
ENST00000652036.1:c.297C>T
|
ENSP00000499139.1:p.Asn99=
|
|
ENST00000652154.1:n.570C>T
|
|
|
ENST00000295497.11:c.297C>T
|
ENSP00000295497.7:p.Asn99=
|
|
ENST00000409089.6:c.-4C>T
|
ENSP00000386322.2:n.-4C>T
|
|
ENST00000409156.7:c.594C>T
|
ENSP00000386470.3:p.Asn198=
|
|
ENST00000409597.5:c.120C>T
|
ENSP00000386469.1:p.Asn40=
|
|
ENST00000409900.7:c.672C>T
|
ENSP00000386741.3:p.Asn224=
|
|
ENST00000413882.5:c.126C>T
|
ENSP00000410496.1:p.Asn42=
|
|
ENST00000425395.5:c.*223C>T
|
ENSP00000405270.1:n.*223C>T
|
|
ENST00000443238.5:c.150C>T
|
ENSP00000409798.1:p.Asn50=
|
|
ENST00000444394.5:c.-4C>T
|
ENSP00000411911.1:n.-4C>T
|
|
ENST00000444573.1:c.297C>T
|
ENSP00000392603.1:p.Asn99=
|
|
ENST00000485882.1:n.131C>T
|
|
|
ENST00000488080.5:n.523C>T
|
|
|
NM_001025201.3:c.594C>T
|
NP_001020372.2:p.Asn198=
|
|
NM_001206602.1:c.297C>T
|
NP_001193531.1:p.Asn99=
|
|
NM_001822.5:c.672C>T
|
NP_001813.1:p.Asn224=
|
|
NR_038133.1:n.538C>T
|
|
|
NM_001025201.4:c.594C>T
|
NP_001020372.2:p.Asn198=
|
|
NM_001206602.2:c.297C>T
|
NP_001193531.1:p.Asn99=
|
|
NM_001371513.1:c.672C>T
|
NP_001358442.1:p.Asn224=
|
|
NM_001371514.1:c.723C>T
|
NP_001358443.1:p.Asn241=
|
|
NM_001822.7:c.672C>T
MANE Select
|
NP_001813.1:p.Asn224=
|
|
NR_038133.2:n.540C>T
|
|
|