ENST00000496887.7:c.1209C=
|
ENSP00000434560.2:p.Tyr403=
|
|
ENST00000646564.2:c.1026C=
|
ENSP00000495806.2:p.Tyr342=
|
|
ENST00000155840.12:c.1566C=
MANE Select
|
ENSP00000155840.2:p.Tyr522=
|
|
ENST00000335475.6:c.1185C=
|
ENSP00000334497.5:p.Tyr395=
|
|
ENST00000646564.1:c.672C=
|
ENSP00000495806.1:p.Tyr224=
|
|
ENST00000155840.9:c.1566C=
|
ENSP00000155840.2:p.Tyr522=
|
|
ENST00000335475.5:c.1185C=
|
ENSP00000334497.5:p.Tyr395=
|
|
NM_000218.2:c.1566C= , LRG_287t1:c.1566C=
|
NP_000209.2:p.Tyr522=
|
|
NM_181798.1:c.1185C= , LRG_287t2:c.1185C=
|
NP_861463.1:p.Tyr395=
|
|
NM_000218.3:c.1566C=
MANE Select
|
NP_000209.2:p.Tyr522=
|
|