ENST00000337233.9:c.285G>T
MANE Select
|
ENSP00000336607.4:p.Glu95Asp
|
|
ENST00000314442.7:n.4419G>T
|
|
|
ENST00000337233.8:c.285G>T
|
ENSP00000336607.4:p.Glu95Asp
|
|
ENST00000359949.11:c.333G>T
|
ENSP00000353032.7:p.Glu111Asp
|
|
ENST00000499638.6:n.321G>T
|
|
|
ENST00000538417.2:c.215G>T
|
|
|
ENST00000538701.5:c.135-6618G>T
|
ENSP00000444033.1:n.135-6618G>T
|
|
ENST00000540930.5:n.321G>T
|
|
|
ENST00000541187.5:n.131G>T
|
|
|
ENST00000542067.5:c.285G>T
|
ENSP00000438329.1:p.Glu95Asp
|
|
ENST00000543171.5:c.285G>T
|
ENSP00000438131.2:p.Glu95Asp
|
|
ENST00000543318.5:c.285G>T
|
ENSP00000444274.1:p.Glu95Asp
|
|
ENST00000543430.5:n.333G>T
|
|
|
ENST00000543984.5:c.137G>T
|
ENSP00000439386.1:p.Arg46Met
|
|
NM_001256796.1:c.333G>T
|
NP_001243725.1:p.Glu111Asp
|
|
NM_001261397.1:c.285G>T
|
NP_001248326.1:p.Glu95Asp
|
|
NM_001261398.1:c.285G>T
|
NP_001248327.1:p.Glu95Asp
|
|
NM_002560.2:c.285G>T
|
NP_002551.2:p.Glu95Asp
|
|
NR_046372.1:n.589G>T
|
|
|
NR_046373.1:n.441G>T
|
|
|
XM_011538416.1:c.135-6618G>T
|
XP_011536718.1:n.135-6618G>T
|
|
XM_011538417.1:c.333G>T
|
XP_011536719.1:p.Glu111Asp
|
|
XR_944559.1:n.393G>T
|
|
|
XM_011538416.2:c.135-6618G>T
|
XP_011536718.1:n.135-6618G>T
|
|
XR_001748726.2:n.339G>T
|
|
|
XR_001748727.1:n.402G>T
|
|
|
XR_001748728.1:n.402G>T
|
|
|
XR_001748729.2:n.339G>T
|
|
|
XR_944559.2:n.392G>T
|
|
|
NM_001256796.2:c.333G>T
|
NP_001243725.1:p.Glu111Asp
|
|
NM_001261397.2:c.285G>T
|
NP_001248326.1:p.Glu95Asp
|
|
NM_001261398.2:c.285G>T
|
NP_001248327.1:p.Glu95Asp
|
|
NM_002560.3:c.285G>T
MANE Select
|
NP_002551.2:p.Glu95Asp
|
|
NR_046372.2:n.321G>T
|
|
|
NR_046373.2:n.173G>T
|
|
|