NM_003242.6:c.1006T=
MANE Select
|
NP_003233.4:p.Tyr336=
|
ENST00000295754.10:c.1006T=
MANE Select
|
ENSP00000295754.5:p.Tyr336=
|
NM_001024847.2:c.1081T= , LRG_779t1:c.1081T=
|
NP_001020018.1:p.Tyr361=
|
NM_003242.5:c.1006T=
|
NP_003233.4:p.Tyr336=
|
ENST00000295754.9:c.1006T=
|
ENSP00000295754.5:p.Tyr336=
|
ENST00000359013.4:c.1081T=
|
ENSP00000351905.4:p.Tyr361=
|
ENST00000672866.1:n.2602T=
|
|
XM_011534043.1:c.1033T=
|
XP_011532345.1:p.Tyr345=
|
XM_011534043.2:c.1033T=
|
XP_011532345.1:p.Tyr345=
|
XM_011534044.1:c.958T=
|
XP_011532346.1:p.Tyr320=
|
XM_011534045.1:c.901T=
|
XP_011532347.1:p.Tyr301=
|
XM_011534045.3:c.901T=
|
XP_011532347.1:p.Tyr301=
|
XM_017007106.1:c.901T=
|
XP_016862595.1:p.Tyr301=
|