ENST00000295497.13:c.330A>G
|
ENSP00000295497.7:p.Lys110=
|
|
ENST00000444394.7:c.330A>G
|
ENSP00000411911.2:p.Lys110=
|
|
ENST00000295497.12:c.330A>G
|
ENSP00000295497.7:p.Lys110=
|
|
ENST00000409089.7:c.30A>G
|
ENSP00000386322.3:p.Lys10=
|
|
ENST00000409900.9:c.705A>G
MANE Select
|
ENSP00000386741.4:p.Lys235=
|
|
ENST00000413882.6:c.159A>G
|
ENSP00000410496.2:p.Lys53=
|
|
ENST00000425395.6:c.*152A>G
|
ENSP00000405270.2:n.*152A>G
|
|
ENST00000443238.6:c.183A>G
|
ENSP00000409798.2:p.Lys61=
|
|
ENST00000444394.6:c.330A>G
|
ENSP00000411911.2:p.Lys110=
|
|
ENST00000444573.2:c.549A>G
|
ENSP00000392603.2:p.Lys183=
|
|
ENST00000488080.6:n.348A>G
|
|
|
ENST00000650731.1:c.30A>G
|
ENSP00000499146.1:p.Lys10=
|
|
ENST00000650938.1:c.229A>G
|
|
|
ENST00000651246.1:c.297A>G
|
ENSP00000498484.1:p.Lys99=
|
|
ENST00000651373.1:c.219A>G
|
ENSP00000499174.1:p.Lys73=
|
|
ENST00000651501.1:c.*152A>G
|
ENSP00000498894.1:n.*152A>G
|
|
ENST00000651717.1:c.253-11959A>G
|
ENSP00000499124.1:n.253-11959A>G
|
|
ENST00000652036.1:c.330A>G
|
ENSP00000499139.1:p.Lys110=
|
|
ENST00000652154.1:n.603A>G
|
|
|
ENST00000295497.11:c.330A>G
|
ENSP00000295497.7:p.Lys110=
|
|
ENST00000409089.6:c.30A>G
|
ENSP00000386322.2:p.Lys10=
|
|
ENST00000409156.7:c.627A>G
|
ENSP00000386470.3:p.Lys209=
|
|
ENST00000409597.5:c.153A>G
|
ENSP00000386469.1:p.Lys51=
|
|
ENST00000409900.7:c.705A>G
|
ENSP00000386741.3:p.Lys235=
|
|
ENST00000413882.5:c.159A>G
|
ENSP00000410496.1:p.Lys53=
|
|
ENST00000425395.5:c.*256A>G
|
ENSP00000405270.1:n.*256A>G
|
|
ENST00000443238.5:c.183A>G
|
ENSP00000409798.1:p.Lys61=
|
|
ENST00000444394.5:c.30A>G
|
ENSP00000411911.1:p.Lys10=
|
|
ENST00000444573.1:c.330A>G
|
ENSP00000392603.1:p.Lys110=
|
|
ENST00000485882.1:n.164A>G
|
|
|
ENST00000488080.5:n.556A>G
|
|
|
NM_001025201.3:c.627A>G
|
NP_001020372.2:p.Lys209=
|
|
NM_001206602.1:c.330A>G
|
NP_001193531.1:p.Lys110=
|
|
NM_001822.5:c.705A>G
|
NP_001813.1:p.Lys235=
|
|
NR_038133.1:n.571A>G
|
|
|
NM_001025201.4:c.627A>G
|
NP_001020372.2:p.Lys209=
|
|
NM_001206602.2:c.330A>G
|
NP_001193531.1:p.Lys110=
|
|
NM_001371513.1:c.705A>G
|
NP_001358442.1:p.Lys235=
|
|
NM_001371514.1:c.756A>G
|
NP_001358443.1:p.Lys252=
|
|
NM_001822.7:c.705A>G
MANE Select
|
NP_001813.1:p.Lys235=
|
|
NR_038133.2:n.573A>G
|
|
|