ENST00000480188.2:n.1521A=
|
|
|
ENST00000696279.1:c.4807A=
|
|
|
ENST00000696280.1:n.4576A=
|
|
|
ENST00000696281.1:c.4505A=
|
ENSP00000512521.1:p.Tyr1502=
|
|
ENST00000697921.1:n.3365A=
|
|
|
ENST00000697922.1:c.*4477A=
|
ENSP00000513478.1:n.*4477A=
|
|
ENST00000697923.1:n.4932A=
|
|
|
ENST00000223642.3:c.4487A=
MANE Select
|
ENSP00000223642.1:p.Tyr1496=
|
|
ENST00000223642.2:c.4487A=
|
ENSP00000223642.1:p.Tyr1496=
|
|
ENST00000480188.1:n.20A=
|
|
|
NM_001735.2:c.4487A= , LRG_28t1:c.4487A=
|
NP_001726.2:p.Tyr1496=
|
|
XM_011518980.1:c.4502A=
|
XP_011517282.1:p.Tyr1501=
|
|
NM_001317163.1:c.4505A=
|
NP_001304092.1:p.Tyr1502=
|
|
NM_001317163.2:c.4505A=
|
NP_001304092.1:p.Tyr1502=
|
|
NM_001735.3:c.4487A=
MANE Select
|
NP_001726.2:p.Tyr1496=
|
|