ENST00000218099.7:c.934T=
MANE Select
|
ENSP00000218099.2:p.Tyr312=
|
|
ENST00000643157.1:n.1601T=
|
|
|
ENST00000218099.6:c.934T=
|
ENSP00000218099.2:p.Tyr312=
|
|
ENST00000394090.2:c.820T=
|
ENSP00000377650.2:p.Tyr274=
|
|
NM_000133.3:c.934T= , LRG_556t1:c.934T=
|
NP_000124.1:p.Tyr312=
|
|
NM_001313913.1:c.820T=
|
NP_001300842.1:p.Tyr274=
|
|
XM_005262397.3:c.805T=
|
XP_005262454.1:p.Tyr269=
|
|
XM_005262397.4:c.805T=
|
XP_005262454.1:p.Tyr269=
|
|
NM_000133.4:c.934T=
MANE Select
|
NP_000124.1:p.Tyr312=
|
|
NM_001313913.2:c.820T=
|
NP_001300842.1:p.Tyr274=
|
|