ENST00000357685.11:c.386A>T
MANE Select
|
ENSP00000350314.5:p.Asp129Val
|
|
ENST00000357685.9:c.386A>T
|
ENSP00000350314.5:p.Asp129Val
|
|
ENST00000361053.8:c.386A>T
|
ENSP00000354338.4:p.Asp129Val
|
|
ENST00000438022.5:c.284A>T
|
ENSP00000414843.1:p.Asp95Val
|
|
ENST00000460924.6:n.478A>T
|
|
|
ENST00000494860.5:n.238A>T
|
|
|
ENST00000525468.1:n.375A>T
|
|
|
ENST00000525987.5:n.729A>T
|
|
|
ENST00000526088.5:c.284A>T
|
ENSP00000436615.1:p.Asp95Val
|
|
ENST00000527939.1:c.*28A>T
|
ENSP00000436956.1:n.*28A>T
|
|
ENST00000530677.1:c.93A>T
|
|
|
ENST00000531169.5:c.284A>T
|
ENSP00000437053.1:p.Asp95Val
|
|
ENST00000532593.5:c.71A>T
|
ENSP00000431802.1:p.Asp24Val
|
|
ENST00000532612.5:c.316A>T
|
|
|
ENST00000534122.5:n.1001A>T
|
|
|
ENST00000534550.5:c.*28A>T
|
ENSP00000434488.1:n.*28A>T
|
|
NM_001037290.2:c.284A>T
|
NP_001032367.2:p.Asp95Val
|
|
NM_001256397.1:c.284A>T
|
NP_001243326.1:p.Asp95Val
|
|
NM_001256398.1:c.386A>T
|
NP_001243327.1:p.Asp129Val
|
|
NM_001256400.1:c.71A>T
|
NP_001243329.1:p.Asp24Val
|
|
NM_031938.5:c.386A>T
|
NP_114144.4:p.Asp129Val
|
|
NM_001037290.3:c.284A>T
|
NP_001032367.3:p.Asp95Val
|
|
NM_001256397.2:c.284A>T
|
NP_001243326.2:p.Asp95Val
|
|
NM_001256398.2:c.386A>T
|
NP_001243327.2:p.Asp129Val
|
|
NM_001256400.2:c.71A>T
|
NP_001243329.2:p.Asp24Val
|
|
NM_031938.7:c.386A>T
MANE Select
|
NP_114144.5:p.Asp129Val
|
|
NM_001037290.4:c.284A>T
|
NP_001032367.3:p.Asp95Val
|
|
NM_001256397.3:c.284A>T
|
NP_001243326.2:p.Asp95Val
|
|
NM_001256398.3:c.386A>T
|
NP_001243327.2:p.Asp129Val
|
|
NM_001256400.3:c.71A>T
|
NP_001243329.2:p.Asp24Val
|
|