ENST00000295754.10:c.770A>T
MANE Select
|
ENSP00000295754.5:p.Glu257Val
|
|
ENST00000672866.1:n.2366A>T
|
|
|
ENST00000295754.9:c.770A>T
|
ENSP00000295754.5:p.Glu257Val
|
|
ENST00000359013.4:c.845A>T
|
ENSP00000351905.4:p.Glu282Val
|
|
NM_001024847.2:c.845A>T , LRG_779t1:c.845A>T
|
NP_001020018.1:p.Glu282Val
|
|
NM_003242.5:c.770A>T
|
NP_003233.4:p.Glu257Val
|
|
XM_011534043.1:c.797A>T
|
XP_011532345.1:p.Glu266Val
|
|
XM_011534044.1:c.722A>T
|
XP_011532346.1:p.Glu241Val
|
|
XM_011534045.1:c.665A>T
|
XP_011532347.1:p.Glu222Val
|
|
XM_011534043.2:c.797A>T
|
XP_011532345.1:p.Glu266Val
|
|
XM_011534045.3:c.665A>T
|
XP_011532347.1:p.Glu222Val
|
|
XM_017007106.1:c.665A>T
|
XP_016862595.1:p.Glu222Val
|
|
NM_003242.6:c.770A>T
MANE Select
|
NP_003233.4:p.Glu257Val
|
|