ENST00000258145.8:c.1157T>G
MANE Select
|
ENSP00000258145.3:p.Leu386Arg
|
|
ENST00000258145.7:c.1157T>G
|
ENSP00000258145.3:p.Leu386Arg
|
|
ENST00000418919.6:c.989T>G
|
ENSP00000413130.2:p.Leu330Arg
|
|
ENST00000537823.1:n.156T>G
|
|
|
ENST00000540196.5:c.557-5886T>G
|
|
|
ENST00000540883.1:n.220T>G
|
|
|
ENST00000541781.5:n.1212T>G
|
|
|
ENST00000542058.5:c.1097T>G
|
ENSP00000444819.1:p.Leu366Arg
|
|
ENST00000543646.5:c.1253T>G
|
ENSP00000438497.1:p.Leu418Arg
|
|
NM_002076.3:c.1157T>G
|
NP_002067.1:p.Leu386Arg
|
|
NM_002076.4:c.1157T>G
MANE Select
|
NP_002067.1:p.Leu386Arg
|
|