ENST00000546609.2:n.532T>G
|
|
|
ENST00000713544.1:c.701T>G
|
ENSP00000518840.1:p.Leu234Trp
|
|
ENST00000713545.1:c.678T>G
|
ENSP00000518841.1:p.Leu226=
|
|
ENST00000228606.9:c.620T>G
MANE Select
|
ENSP00000228606.4:p.Leu207Trp
|
|
ENST00000228606.8:c.620T>G
|
ENSP00000228606.4:p.Leu207Trp
|
|
ENST00000546567.5:c.-86T>G
|
ENSP00000449472.1:n.-86T>G
|
|
ENST00000546609.1:c.532T>G
|
|
|
ENST00000547344.5:n.759T>G
|
|
|
ENST00000547451.1:n.420T>G
|
|
|
NM_000785.3:c.620T>G
|
NP_000776.1:p.Leu207Trp
|
|
NM_000785.4:c.620T>G
MANE Select
|
NP_000776.1:p.Leu207Trp
|
|