ENST00000295754.10:c.1298G>T
MANE Select
|
ENSP00000295754.5:p.Arg433Met
|
|
ENST00000672866.1:n.2894G>T
|
|
|
ENST00000673203.1:n.176G>T
|
|
|
ENST00000295754.9:c.1298G>T
|
ENSP00000295754.5:p.Arg433Met
|
|
ENST00000359013.4:c.1373G>T
|
ENSP00000351905.4:p.Arg458Met
|
|
NM_001024847.2:c.1373G>T , LRG_779t1:c.1373G>T
|
NP_001020018.1:p.Arg458Met
|
|
NM_003242.5:c.1298G>T
|
NP_003233.4:p.Arg433Met
|
|
XM_011534043.1:c.1325G>T
|
XP_011532345.1:p.Arg442Met
|
|
XM_011534044.1:c.1250G>T
|
XP_011532346.1:p.Arg417Met
|
|
XM_011534045.1:c.1193G>T
|
XP_011532347.1:p.Arg398Met
|
|
XM_011534043.2:c.1325G>T
|
XP_011532345.1:p.Arg442Met
|
|
XM_011534045.3:c.1193G>T
|
XP_011532347.1:p.Arg398Met
|
|
XM_017007106.1:c.1193G>T
|
XP_016862595.1:p.Arg398Met
|
|
NM_003242.6:c.1298G>T
MANE Select
|
NP_003233.4:p.Arg433Met
|
|