ENST00000686073.1:c.854A>T
|
ENSP00000508901.1:p.Asp285Val
|
|
ENST00000380993.8:c.854A>T
MANE Select
|
ENSP00000370381.3:p.Asp285Val
|
|
ENST00000646012.1:c.992A>T
|
ENSP00000495813.1:p.Asp331Val
|
|
ENST00000647232.1:c.854A>T
|
ENSP00000493875.1:p.Asp285Val
|
|
ENST00000647546.1:c.854A>T
|
ENSP00000495332.1:p.Asp285Val
|
|
ENST00000330289.10:c.854A>T
|
ENSP00000331550.6:p.Asp285Val
|
|
ENST00000380993.7:c.854A>T
|
ENSP00000370381.3:p.Asp285Val
|
|
ENST00000396577.7:c.854A>T
|
ENSP00000379822.3:p.Asp285Val
|
|
ENST00000558252.5:n.4977A>T
|
|
|
ENST00000558405.5:c.854A>T
|
ENSP00000453409.1:p.Asp285Val
|
|
ENST00000559641.5:c.293A>T
|
ENSP00000453230.1:p.Asp98Val
|
|
ENST00000559723.2:n.227A>T
|
|
|
ENST00000560692.5:n.4993A>T
|
|
|
ENST00000561127.5:c.293A>T
|
ENSP00000453602.2:p.Asp98Val
|
|
NM_000338.2:c.854A>T
|
NP_000329.2:p.Asp285Val
|
|
NM_001184832.1:c.854A>T
|
NP_001171761.1:p.Asp285Val
|
|
XM_005254605.1:c.950A>T
|
XP_005254662.1:p.Asp317Val
|
|
XM_005254606.1:c.854A>T
|
XP_005254663.1:p.Asp285Val
|
|
XM_006720656.1:c.950A>T
|
XP_006720719.1:p.Asp317Val
|
|
XR_931896.1:n.1166A>T
|
|
|
XR_932203.1:n.229+638T>A
|
|
|
XR_932204.1:n.222+638T>A
|
|
|
XM_005254606.2:c.854A>T
|
XP_005254663.1:p.Asp285Val
|
|
XR_001751524.2:n.230+638T>A
|
|
|
XR_001751525.1:n.230+638T>A
|
|
|
XR_002957762.1:n.230+638T>A
|
|
|
XR_932204.3:n.224+638T>A
|
|
|
NM_000338.3:c.854A>T
MANE Select
|
NP_000329.2:p.Asp285Val
|
|
NM_001184832.2:c.854A>T
|
NP_001171761.1:p.Asp285Val
|
|
NM_001384136.1:c.854A>T
|
NP_001371065.1:p.Asp285Val
|
|