ENST00000295754.10:c.834C=
MANE Select
|
ENSP00000295754.5:p.Ile278=
|
|
ENST00000672866.1:n.2430C=
|
|
|
ENST00000295754.9:c.834C=
|
ENSP00000295754.5:p.Ile278=
|
|
ENST00000359013.4:c.909C=
|
ENSP00000351905.4:p.Ile303=
|
|
NM_001024847.2:c.909C= , LRG_779t1:c.909C=
|
NP_001020018.1:p.Ile303=
|
|
NM_003242.5:c.834C=
|
NP_003233.4:p.Ile278=
|
|
XM_011534043.1:c.861C=
|
XP_011532345.1:p.Ile287=
|
|
XM_011534044.1:c.786C=
|
XP_011532346.1:p.Ile262=
|
|
XM_011534045.1:c.729C=
|
XP_011532347.1:p.Ile243=
|
|
XM_011534043.2:c.861C=
|
XP_011532345.1:p.Ile287=
|
|
XM_011534045.3:c.729C=
|
XP_011532347.1:p.Ile243=
|
|
XM_017007106.1:c.729C=
|
XP_016862595.1:p.Ile243=
|
|
NM_003242.6:c.834C=
MANE Select
|
NP_003233.4:p.Ile278=
|
|