ENST00000269980.7:c.335T>G
MANE Select
|
ENSP00000269980.2:p.Leu112Arg
|
|
ENST00000269980.6:c.335T>G
|
ENSP00000269980.2:p.Leu112Arg
|
|
ENST00000457836.6:c.269T>G
|
ENSP00000416000.2:p.Leu90Arg
|
|
ENST00000538423.5:n.461T>G
|
|
|
ENST00000540732.3:c.437T>G
|
ENSP00000443246.1:p.Leu146Arg
|
|
ENST00000541315.1:c.142T>G
|
|
|
ENST00000542943.5:c.288+153T>G
|
ENSP00000440345.1:n.288+153T>G
|
|
ENST00000595085.5:c.335T>G
|
ENSP00000471150.2:p.Leu112Arg
|
|
NM_000709.3:c.335T>G
|
NP_000700.1:p.Leu112Arg
|
|
NM_001164783.1:c.335T>G
|
NP_001158255.1:p.Leu112Arg
|
|
NM_000709.4:c.335T>G
MANE Select
|
NP_000700.1:p.Leu112Arg
|
|
NM_001164783.2:c.335T>G
|
NP_001158255.1:p.Leu112Arg
|
|