ENST00000295497.13:c.293C>T
|
ENSP00000295497.7:p.Ala98Val
|
|
ENST00000444394.7:c.293C>T
|
ENSP00000411911.2:p.Ala98Val
|
|
ENST00000295497.12:c.293C>T
|
ENSP00000295497.7:p.Ala98Val
|
|
ENST00000409089.7:c.-8C>T
|
ENSP00000386322.3:n.-8C>T
|
|
ENST00000409900.9:c.668C>T
MANE Select
|
ENSP00000386741.4:p.Ala223Val
|
|
ENST00000413882.6:c.122C>T
|
ENSP00000410496.2:p.Ala41Val
|
|
ENST00000425395.6:c.*115C>T
|
ENSP00000405270.2:n.*115C>T
|
|
ENST00000443238.6:c.146C>T
|
ENSP00000409798.2:p.Ala49Val
|
|
ENST00000444394.6:c.293C>T
|
ENSP00000411911.2:p.Ala98Val
|
|
ENST00000444573.2:c.512C>T
|
ENSP00000392603.2:p.Ala171Val
|
|
ENST00000488080.6:n.311C>T
|
|
|
ENST00000650731.1:c.-8C>T
|
ENSP00000499146.1:n.-8C>T
|
|
ENST00000650938.1:c.192C>T
|
|
|
ENST00000651246.1:c.260C>T
|
ENSP00000498484.1:p.Ala87Val
|
|
ENST00000651373.1:c.182C>T
|
ENSP00000499174.1:p.Ala61Val
|
|
ENST00000651501.1:c.*115C>T
|
ENSP00000498894.1:n.*115C>T
|
|
ENST00000651717.1:c.253-11996C>T
|
ENSP00000499124.1:n.253-11996C>T
|
|
ENST00000652036.1:c.293C>T
|
ENSP00000499139.1:p.Ala98Val
|
|
ENST00000652154.1:n.566C>T
|
|
|
ENST00000295497.11:c.293C>T
|
ENSP00000295497.7:p.Ala98Val
|
|
ENST00000409089.6:c.-8C>T
|
ENSP00000386322.2:n.-8C>T
|
|
ENST00000409156.7:c.590C>T
|
ENSP00000386470.3:p.Ala197Val
|
|
ENST00000409597.5:c.116C>T
|
ENSP00000386469.1:p.Ala39Val
|
|
ENST00000409900.7:c.668C>T
|
ENSP00000386741.3:p.Ala223Val
|
|
ENST00000413882.5:c.122C>T
|
ENSP00000410496.1:p.Ala41Val
|
|
ENST00000425395.5:c.*219C>T
|
ENSP00000405270.1:n.*219C>T
|
|
ENST00000443238.5:c.146C>T
|
ENSP00000409798.1:p.Ala49Val
|
|
ENST00000444394.5:c.-8C>T
|
ENSP00000411911.1:n.-8C>T
|
|
ENST00000444573.1:c.293C>T
|
ENSP00000392603.1:p.Ala98Val
|
|
ENST00000485882.1:n.127C>T
|
|
|
ENST00000488080.5:n.519C>T
|
|
|
NM_001025201.3:c.590C>T
|
NP_001020372.2:p.Ala197Val
|
|
NM_001206602.1:c.293C>T
|
NP_001193531.1:p.Ala98Val
|
|
NM_001822.5:c.668C>T
|
NP_001813.1:p.Ala223Val
|
|
NR_038133.1:n.534C>T
|
|
|
NM_001025201.4:c.590C>T
|
NP_001020372.2:p.Ala197Val
|
|
NM_001206602.2:c.293C>T
|
NP_001193531.1:p.Ala98Val
|
|
NM_001371513.1:c.668C>T
|
NP_001358442.1:p.Ala223Val
|
|
NM_001371514.1:c.719C>T
|
NP_001358443.1:p.Ala240Val
|
|
NM_001822.7:c.668C>T
MANE Select
|
NP_001813.1:p.Ala223Val
|
|
NR_038133.2:n.536C>T
|
|
|