ENST00000480188.2:n.1432G>T
|
|
|
ENST00000696279.1:c.4718G>T
|
|
|
ENST00000696280.1:n.4487G>T
|
|
|
ENST00000696281.1:c.4416G>T
|
ENSP00000512521.1:p.Ser1472=
|
|
ENST00000697921.1:n.3276G>T
|
|
|
ENST00000697922.1:c.*4388G>T
|
ENSP00000513478.1:n.*4388G>T
|
|
ENST00000697923.1:n.4843G>T
|
|
|
ENST00000223642.3:c.4398G>T
MANE Select
|
ENSP00000223642.1:p.Ser1466=
|
|
ENST00000223642.2:c.4398G>T
|
ENSP00000223642.1:p.Ser1466=
|
|
NM_001735.2:c.4398G>T , LRG_28t1:c.4398G>T
|
NP_001726.2:p.Ser1466=
|
|
XM_011518980.1:c.4413G>T
|
XP_011517282.1:p.Ser1471=
|
|
NM_001317163.1:c.4416G>T
|
NP_001304092.1:p.Ser1472=
|
|
NM_001317163.2:c.4416G>T
|
NP_001304092.1:p.Ser1472=
|
|
NM_001735.3:c.4398G>T
MANE Select
|
NP_001726.2:p.Ser1466=
|
|