ENST00000399391.7:c.373T>G
|
ENSP00000382323.2:p.Phe125Val
|
|
ENST00000399397.6:c.337T>G
MANE Select
|
ENSP00000382329.2:p.Phe113Val
|
|
ENST00000399391.6:c.373T>G
|
ENSP00000382323.2:p.Phe125Val
|
|
ENST00000399397.5:c.337T>G
|
ENSP00000382329.2:p.Phe113Val
|
|
ENST00000428619.1:c.154T>G
|
ENSP00000399057.2:p.Phe52Val
|
|
ENST00000498332.5:n.243T>G
|
|
|
NM_001277269.1:c.373T>G
|
NP_001264198.1:p.Phe125Val
|
|
NM_001292063.1:c.337T>G
|
NP_001278992.1:p.Phe113Val
|
|
NM_001277269.2:c.373T>G
|
NP_001264198.1:p.Phe125Val
|
|
NM_001292063.2:c.337T>G
MANE Select
|
NP_001278992.1:p.Phe113Val
|
|