ENST00000295497.13:c.333T>A
|
ENSP00000295497.7:p.Cys111Ter
|
|
ENST00000444394.7:c.333T>A
|
ENSP00000411911.2:p.Cys111Ter
|
|
ENST00000295497.12:c.333T>A
|
ENSP00000295497.7:p.Cys111Ter
|
|
ENST00000409089.7:c.33T>A
|
ENSP00000386322.3:p.Cys11Ter
|
|
ENST00000409900.9:c.708T>A
MANE Select
|
ENSP00000386741.4:p.Cys236Ter
|
|
ENST00000413882.6:c.162T>A
|
ENSP00000410496.2:p.Cys54Ter
|
|
ENST00000425395.6:c.*155T>A
|
ENSP00000405270.2:n.*155T>A
|
|
ENST00000443238.6:c.186T>A
|
ENSP00000409798.2:p.Cys62Ter
|
|
ENST00000444394.6:c.333T>A
|
ENSP00000411911.2:p.Cys111Ter
|
|
ENST00000444573.2:c.552T>A
|
ENSP00000392603.2:p.Cys184Ter
|
|
ENST00000488080.6:n.351T>A
|
|
|
ENST00000650731.1:c.33T>A
|
ENSP00000499146.1:p.Cys11Ter
|
|
ENST00000650938.1:c.232T>A
|
|
|
ENST00000651246.1:c.300T>A
|
ENSP00000498484.1:p.Cys100Ter
|
|
ENST00000651373.1:c.222T>A
|
ENSP00000499174.1:p.Cys74Ter
|
|
ENST00000651501.1:c.*155T>A
|
ENSP00000498894.1:n.*155T>A
|
|
ENST00000651717.1:c.253-11956T>A
|
ENSP00000499124.1:n.253-11956T>A
|
|
ENST00000652036.1:c.333T>A
|
ENSP00000499139.1:p.Cys111Ter
|
|
ENST00000652154.1:n.606T>A
|
|
|
ENST00000295497.11:c.333T>A
|
ENSP00000295497.7:p.Cys111Ter
|
|
ENST00000409089.6:c.33T>A
|
ENSP00000386322.2:p.Cys11Ter
|
|
ENST00000409156.7:c.630T>A
|
ENSP00000386470.3:p.Cys210Ter
|
|
ENST00000409597.5:c.156T>A
|
ENSP00000386469.1:p.Cys52Ter
|
|
ENST00000409900.7:c.708T>A
|
ENSP00000386741.3:p.Cys236Ter
|
|
ENST00000413882.5:c.162T>A
|
ENSP00000410496.1:p.Cys54Ter
|
|
ENST00000425395.5:c.*259T>A
|
ENSP00000405270.1:n.*259T>A
|
|
ENST00000443238.5:c.186T>A
|
ENSP00000409798.1:p.Cys62Ter
|
|
ENST00000444394.5:c.33T>A
|
ENSP00000411911.1:p.Cys11Ter
|
|
ENST00000444573.1:c.333T>A
|
ENSP00000392603.1:p.Cys111Ter
|
|
ENST00000485882.1:n.167T>A
|
|
|
ENST00000488080.5:n.559T>A
|
|
|
NM_001025201.3:c.630T>A
|
NP_001020372.2:p.Cys210Ter
|
|
NM_001206602.1:c.333T>A
|
NP_001193531.1:p.Cys111Ter
|
|
NM_001822.5:c.708T>A
|
NP_001813.1:p.Cys236Ter
|
|
NR_038133.1:n.574T>A
|
|
|
NM_001025201.4:c.630T>A
|
NP_001020372.2:p.Cys210Ter
|
|
NM_001206602.2:c.333T>A
|
NP_001193531.1:p.Cys111Ter
|
|
NM_001371513.1:c.708T>A
|
NP_001358442.1:p.Cys236Ter
|
|
NM_001371514.1:c.759T>A
|
NP_001358443.1:p.Cys253Ter
|
|
NM_001822.7:c.708T>A
MANE Select
|
NP_001813.1:p.Cys236Ter
|
|
NR_038133.2:n.576T>A
|
|
|