ENST00000295497.13:c.922G>T
|
ENSP00000295497.7:p.Asp308Tyr
|
|
ENST00000295497.12:c.922G>T
|
ENSP00000295497.7:p.Asp308Tyr
|
|
ENST00000409900.9:c.1297G>T
MANE Select
|
ENSP00000386741.4:p.Asp433Tyr
|
|
ENST00000413882.6:c.751G>T
|
ENSP00000410496.2:p.Asp251Tyr
|
|
ENST00000443238.6:c.775G>T
|
ENSP00000409798.2:p.Asp259Tyr
|
|
ENST00000488080.6:n.940G>T
|
|
|
ENST00000650731.1:c.622G>T
|
ENSP00000499146.1:p.Asp208Tyr
|
|
ENST00000650938.1:c.683G>T
|
|
|
ENST00000651246.1:c.889G>T
|
ENSP00000498484.1:p.Asp297Tyr
|
|
ENST00000651501.1:c.*744G>T
|
ENSP00000498894.1:n.*744G>T
|
|
ENST00000651717.1:c.*573G>T
|
ENSP00000499124.1:n.*573G>T
|
|
ENST00000652036.1:c.973G>T
|
ENSP00000499139.1:p.Asp325Tyr
|
|
ENST00000295497.11:c.922G>T
|
ENSP00000295497.7:p.Asp308Tyr
|
|
ENST00000409156.7:c.1219G>T
|
ENSP00000386470.3:p.Asp407Tyr
|
|
ENST00000409597.5:c.745G>T
|
ENSP00000386469.1:p.Asp249Tyr
|
|
ENST00000409900.7:c.1297G>T
|
ENSP00000386741.3:p.Asp433Tyr
|
|
ENST00000488080.5:n.1148G>T
|
|
|
ENST00000492964.1:n.440G>T
|
|
|
NM_001025201.3:c.1219G>T
|
NP_001020372.2:p.Asp407Tyr
|
|
NM_001206602.1:c.922G>T
|
NP_001193531.1:p.Asp308Tyr
|
|
NM_001822.5:c.1297G>T
|
NP_001813.1:p.Asp433Tyr
|
|
NR_038133.1:n.1163G>T
|
|
|
NM_001025201.4:c.1219G>T
|
NP_001020372.2:p.Asp407Tyr
|
|
NM_001206602.2:c.922G>T
|
NP_001193531.1:p.Asp308Tyr
|
|
NM_001371513.1:c.1297G>T
|
NP_001358442.1:p.Asp433Tyr
|
|
NM_001371514.1:c.1348G>T
|
NP_001358443.1:p.Asp450Tyr
|
|
NM_001822.7:c.1297G>T
MANE Select
|
NP_001813.1:p.Asp433Tyr
|
|
NR_038133.2:n.1165G>T
|
|
|