ENST00000388922.9:c.1383C>T
MANE Select
|
ENSP00000373574.4:p.Leu461=
|
|
ENST00000388922.8:c.1383C>T
|
ENSP00000373574.4:p.Leu461=
|
|
ENST00000419526.6:c.861C>T
|
ENSP00000392492.2:p.Leu287=
|
|
ENST00000550683.5:c.1425C>T
|
ENSP00000447884.1:p.Leu475=
|
|
NM_000020.2:c.1383C>T , LRG_543t1:c.1383C>T
|
NP_000011.2:p.Leu461=
|
|
NM_001077401.1:c.1383C>T
|
NP_001070869.1:p.Leu461=
|
|
XM_005269235.2:c.1383C>T
|
XP_005269292.1:p.Leu461=
|
|
XM_011539008.1:c.1113C>T
|
XP_011537310.1:p.Leu371=
|
|
XM_024449279.1:c.594C>T
|
XP_024305047.1:p.Leu198=
|
|
NM_000020.3:c.1383C>T
MANE Select
|
NP_000011.2:p.Leu461=
|
|
NM_001077401.2:c.1383C>T
|
NP_001070869.1:p.Leu461=
|
|