ENST00000330062.8:c.445C>T
MANE Select
|
ENSP00000331897.4:p.Arg149Trp
|
|
ENST00000330062.7:c.445C>T
|
ENSP00000331897.3:p.Arg149Trp
|
|
ENST00000540499.2:c.289C>T
|
ENSP00000446147.2:p.Arg97Trp
|
|
ENST00000559482.5:c.208-174C>T
|
ENSP00000453016.1:n.208-174C>T
|
|
ENST00000560061.1:c.*70C>T
|
ENSP00000453254.1:n.*70C>T
|
|
NM_001289910.1:c.289C>T , LRG_611t1:c.289C>T
|
NP_001276839.1:p.Arg97Trp
|
|
NM_001290114.1:c.55C>T
|
NP_001277043.1:p.Arg19Trp
|
|
NM_002168.3:c.445C>T , LRG_611t2:c.445C>T
|
NP_002159.2:p.Arg149Trp
|
|
NM_001290114.2:c.55C>T
|
NP_001277043.1:p.Arg19Trp
|
|
NM_002168.4:c.445C>T
MANE Select
|
NP_002159.2:p.Arg149Trp
|
|