ENST00000262133.11:c.2594G>T
MANE Select
|
ENSP00000262133.6:p.Arg865Met
|
|
ENST00000680543.1:n.4385G>T
|
|
|
ENST00000262133.10:c.2594G>T
|
ENSP00000262133.6:p.Arg865Met
|
|
ENST00000379935.8:n.2293G>T
|
|
|
ENST00000544545.2:c.1724G>T
|
ENSP00000444685.2:p.Arg575Met
|
|
NM_005611.3:c.2594G>T
|
NP_005602.3:p.Arg865Met
|
|
XM_005256083.3:c.2372G>T
|
XP_005256140.1:p.Arg791Met
|
|
XM_011523252.1:c.2594G>T
|
XP_011521554.1:p.Arg865Met
|
|
XM_011523253.1:c.1946G>T
|
XP_011521555.1:p.Arg649Met
|
|
NM_001323608.1:c.2594G>T
|
NP_001310537.1:p.Arg865Met
|
|
NM_001323609.1:c.2594G>T
|
NP_001310538.1:p.Arg865Met
|
|
NM_001323610.1:c.2447G>T
|
NP_001310539.1:p.Arg816Met
|
|
NM_001323611.1:c.2372G>T
|
NP_001310540.1:p.Arg791Met
|
|
XM_011523253.2:c.1946G>T
|
XP_011521555.1:p.Arg649Met
|
|
XM_017023513.1:c.1946G>T
|
XP_016879002.1:p.Arg649Met
|
|
NM_005611.4:c.2594G>T
MANE Select
|
NP_005602.3:p.Arg865Met
|
|
NM_001323608.2:c.2594G>T
|
NP_001310537.1:p.Arg865Met
|
|
NM_001323609.2:c.2594G>T
|
NP_001310538.1:p.Arg865Met
|
|
NM_001323610.2:c.2447G>T
|
NP_001310539.1:p.Arg816Met
|
|