ENST00000546609.2:n.535G>C
|
|
|
ENST00000713544.1:c.704G>C
|
ENSP00000518840.1:p.Gly235Ala
|
|
ENST00000713545.1:c.681G>C
|
ENSP00000518841.1:p.Gly227=
|
|
ENST00000228606.9:c.623G>C
MANE Select
|
ENSP00000228606.4:p.Gly208Ala
|
|
ENST00000228606.8:c.623G>C
|
ENSP00000228606.4:p.Gly208Ala
|
|
ENST00000546567.5:c.-83G>C
|
ENSP00000449472.1:n.-83G>C
|
|
ENST00000546609.1:c.535G>C
|
|
|
ENST00000547344.5:n.762G>C
|
|
|
ENST00000547451.1:n.423G>C
|
|
|
NM_000785.3:c.623G>C
|
NP_000776.1:p.Gly208Ala
|
|
NM_000785.4:c.623G>C
MANE Select
|
NP_000776.1:p.Gly208Ala
|
|