ENST00000546609.2:n.682G>A
|
|
|
ENST00000713544.1:c.851G>A
|
ENSP00000518840.1:p.Trp284Ter
|
|
ENST00000713545.1:c.828G>A
|
ENSP00000518841.1:p.Leu276=
|
|
ENST00000228606.9:c.770G>A
MANE Select
|
ENSP00000228606.4:p.Trp257Ter
|
|
ENST00000228606.8:c.770G>A
|
ENSP00000228606.4:p.Trp257Ter
|
|
ENST00000546567.5:c.65G>A
|
ENSP00000449472.1:p.Trp22Ter
|
|
ENST00000546609.1:c.682G>A
|
|
|
ENST00000547344.5:n.909G>A
|
|
|
ENST00000547451.1:n.570G>A
|
|
|
NM_000785.3:c.770G>A
|
NP_000776.1:p.Trp257Ter
|
|
NM_000785.4:c.770G>A
MANE Select
|
NP_000776.1:p.Trp257Ter
|
|