ENST00000294304.12:c.2030C>T
MANE Select
|
ENSP00000294304.6:p.Ala677Val
|
|
ENST00000294304.11:c.2030C>T
|
ENSP00000294304.6:p.Ala677Val
|
|
ENST00000529993.5:c.*636C>T
|
ENSP00000436652.1:n.*636C>T
|
|
NM_001291902.1:c.287C>T
|
NP_001278831.1:p.Ala96Val
|
|
NM_002335.3:c.2030C>T
|
NP_002326.2:p.Ala677Val
|
|
XM_005273994.2:c.2030C>T
|
XP_005274051.1:p.Ala677Val
|
|
XM_011545029.1:c.2057C>T
|
XP_011543331.1:p.Ala686Val
|
|
XM_011545030.1:c.2057C>T
|
XP_011543332.1:p.Ala686Val
|
|
XM_011545031.1:c.2057C>T
|
XP_011543333.1:p.Ala686Val
|
|
XR_949925.1:n.2072C>T
|
|
|
XR_949926.1:n.2072C>T
|
|
|
XM_017017735.1:c.287C>T
|
XP_016873224.1:p.Ala96Val
|
|
XR_001747874.1:n.2072C>T
|
|
|
XR_949925.2:n.2072C>T
|
|
|
XR_949926.2:n.2072C>T
|
|
|
NM_002335.4:c.2030C>T
MANE Select
|
NP_002326.2:p.Ala677Val
|
|
NM_001291902.2:c.287C>T
|
NP_001278831.1:p.Ala96Val
|
|