|
NM_000709.4:c.1061G>A
MANE Select
|
NP_000700.1:p.Trp354Ter
|
|
ENST00000269980.7:c.1061G>A
MANE Select
|
ENSP00000269980.2:p.Trp354Ter
|
|
NM_000709.3:c.1061G>A
|
NP_000700.1:p.Trp354Ter
|
|
NM_001164783.1:c.1058G>A
|
NP_001158255.1:p.Trp353Ter
|
|
NM_001164783.2:c.1058G>A
|
NP_001158255.1:p.Trp353Ter
|
|
ENST00000269980.6:c.1061G>A
|
ENSP00000269980.2:p.Trp354Ter
|
|
ENST00000457836.6:c.1070G>A
|
ENSP00000416000.2:p.Trp357Ter
|
|
ENST00000540732.3:c.1163G>A
|
ENSP00000443246.1:p.Trp388Ter
|
|
ENST00000542943.5:c.974G>A
|
ENSP00000440345.1:p.Trp325Ter
|
|
ENST00000595085.5:c.922+366G>A
|
ENSP00000471150.2:n.922+366G>A
|