ENST00000480188.2:n.1513C>T
|
|
|
ENST00000696279.1:c.4799C>T
|
|
|
ENST00000696280.1:n.4568C>T
|
|
|
ENST00000696281.1:c.4497C>T
|
ENSP00000512521.1:p.Phe1499=
|
|
ENST00000697921.1:n.3357C>T
|
|
|
ENST00000697922.1:c.*4469C>T
|
ENSP00000513478.1:n.*4469C>T
|
|
ENST00000697923.1:n.4924C>T
|
|
|
ENST00000223642.3:c.4479C>T
MANE Select
|
ENSP00000223642.1:p.Phe1493=
|
|
ENST00000223642.2:c.4479C>T
|
ENSP00000223642.1:p.Phe1493=
|
|
ENST00000480188.1:n.12C>T
|
|
|
NM_001735.2:c.4479C>T , LRG_28t1:c.4479C>T
|
NP_001726.2:p.Phe1493=
|
|
XM_011518980.1:c.4494C>T
|
XP_011517282.1:p.Phe1498=
|
|
NM_001317163.1:c.4497C>T
|
NP_001304092.1:p.Phe1499=
|
|
NM_001317163.2:c.4497C>T
|
NP_001304092.1:p.Phe1499=
|
|
NM_001735.3:c.4479C>T
MANE Select
|
NP_001726.2:p.Phe1493=
|
|