|
NM_000709.4:c.1087C>T
MANE Select
|
NP_000700.1:p.Arg363Trp
|
|
ENST00000269980.7:c.1087C>T
MANE Select
|
ENSP00000269980.2:p.Arg363Trp
|
|
NM_000709.3:c.1087C>T
|
NP_000700.1:p.Arg363Trp
|
|
NM_001164783.1:c.1084C>T
|
NP_001158255.1:p.Arg362Trp
|
|
NM_001164783.2:c.1084C>T
|
NP_001158255.1:p.Arg362Trp
|
|
ENST00000269980.6:c.1087C>T
|
ENSP00000269980.2:p.Arg363Trp
|
|
ENST00000457836.6:c.1096C>T
|
ENSP00000416000.2:p.Arg366Trp
|
|
ENST00000540732.3:c.1189C>T
|
ENSP00000443246.1:p.Arg397Trp
|
|
ENST00000595085.5:c.922+392C>T
|
ENSP00000471150.2:n.922+392C>T
|