ENST00000295497.13:c.931G>T
|
ENSP00000295497.7:p.Ala311Ser
|
|
ENST00000295497.12:c.931G>T
|
ENSP00000295497.7:p.Ala311Ser
|
|
ENST00000409900.9:c.1306G>T
MANE Select
|
ENSP00000386741.4:p.Ala436Ser
|
|
ENST00000413882.6:c.760G>T
|
ENSP00000410496.2:p.Ala254Ser
|
|
ENST00000443238.6:c.784G>T
|
ENSP00000409798.2:p.Ala262Ser
|
|
ENST00000488080.6:n.949G>T
|
|
|
ENST00000650731.1:c.631G>T
|
ENSP00000499146.1:p.Ala211Ser
|
|
ENST00000650938.1:c.692G>T
|
|
|
ENST00000651246.1:c.898G>T
|
ENSP00000498484.1:p.Ala300Ser
|
|
ENST00000651501.1:c.*753G>T
|
ENSP00000498894.1:n.*753G>T
|
|
ENST00000651717.1:c.*582G>T
|
ENSP00000499124.1:n.*582G>T
|
|
ENST00000652036.1:c.982G>T
|
ENSP00000499139.1:p.Ala328Ser
|
|
ENST00000295497.11:c.931G>T
|
ENSP00000295497.7:p.Ala311Ser
|
|
ENST00000409156.7:c.1228G>T
|
ENSP00000386470.3:p.Ala410Ser
|
|
ENST00000409597.5:c.754G>T
|
ENSP00000386469.1:p.Ala252Ser
|
|
ENST00000409900.7:c.1306G>T
|
ENSP00000386741.3:p.Ala436Ser
|
|
ENST00000488080.5:n.1157G>T
|
|
|
ENST00000492964.1:n.449G>T
|
|
|
NM_001025201.3:c.1228G>T
|
NP_001020372.2:p.Ala410Ser
|
|
NM_001206602.1:c.931G>T
|
NP_001193531.1:p.Ala311Ser
|
|
NM_001822.5:c.1306G>T
|
NP_001813.1:p.Ala436Ser
|
|
NR_038133.1:n.1172G>T
|
|
|
NM_001025201.4:c.1228G>T
|
NP_001020372.2:p.Ala410Ser
|
|
NM_001206602.2:c.931G>T
|
NP_001193531.1:p.Ala311Ser
|
|
NM_001371513.1:c.1306G>T
|
NP_001358442.1:p.Ala436Ser
|
|
NM_001371514.1:c.1357G>T
|
NP_001358443.1:p.Ala453Ser
|
|
NM_001822.7:c.1306G>T
MANE Select
|
NP_001813.1:p.Ala436Ser
|
|
NR_038133.2:n.1174G>T
|
|
|