ENST00000294304.12:c.2291G>T
MANE Select
|
ENSP00000294304.6:p.Arg764Met
|
|
ENST00000294304.11:c.2291G>T
|
ENSP00000294304.6:p.Arg764Met
|
|
ENST00000528714.1:n.85G>T
|
|
|
ENST00000529993.5:c.*897G>T
|
ENSP00000436652.1:n.*897G>T
|
|
NM_001291902.1:c.548G>T
|
NP_001278831.1:p.Arg183Met
|
|
NM_002335.3:c.2291G>T
|
NP_002326.2:p.Arg764Met
|
|
XM_005273994.2:c.2291G>T
|
XP_005274051.1:p.Arg764Met
|
|
XM_011545029.1:c.2318G>T
|
XP_011543331.1:p.Arg773Met
|
|
XM_011545030.1:c.2318G>T
|
XP_011543332.1:p.Arg773Met
|
|
XM_011545031.1:c.2318G>T
|
XP_011543333.1:p.Arg773Met
|
|
XR_949925.1:n.2333G>T
|
|
|
XR_949926.1:n.2333G>T
|
|
|
XM_017017735.1:c.548G>T
|
XP_016873224.1:p.Arg183Met
|
|
XR_001747874.1:n.2333G>T
|
|
|
XR_949925.2:n.2333G>T
|
|
|
XR_949926.2:n.2333G>T
|
|
|
NM_002335.4:c.2291G>T
MANE Select
|
NP_002326.2:p.Arg764Met
|
|
NM_001291902.2:c.548G>T
|
NP_001278831.1:p.Arg183Met
|
|