ENST00000295754.10:c.948G=
MANE Select
|
ENSP00000295754.5:p.Glu316=
|
|
ENST00000672866.1:n.2544G=
|
|
|
ENST00000295754.9:c.948G=
|
ENSP00000295754.5:p.Glu316=
|
|
ENST00000359013.4:c.1023G=
|
ENSP00000351905.4:p.Glu341=
|
|
NM_001024847.2:c.1023G= , LRG_779t1:c.1023G=
|
NP_001020018.1:p.Glu341=
|
|
NM_003242.5:c.948G=
|
NP_003233.4:p.Glu316=
|
|
XM_011534043.1:c.975G=
|
XP_011532345.1:p.Glu325=
|
|
XM_011534044.1:c.900G=
|
XP_011532346.1:p.Glu300=
|
|
XM_011534045.1:c.843G=
|
XP_011532347.1:p.Glu281=
|
|
XM_011534043.2:c.975G=
|
XP_011532345.1:p.Glu325=
|
|
XM_011534045.3:c.843G=
|
XP_011532347.1:p.Glu281=
|
|
XM_017007106.1:c.843G=
|
XP_016862595.1:p.Glu281=
|
|
NM_003242.6:c.948G=
MANE Select
|
NP_003233.4:p.Glu316=
|
|