ENST00000399391.7:c.343T>G
|
ENSP00000382323.2:p.Phe115Val
|
|
ENST00000399397.6:c.307T>G
MANE Select
|
ENSP00000382329.2:p.Phe103Val
|
|
ENST00000399391.6:c.343T>G
|
ENSP00000382323.2:p.Phe115Val
|
|
ENST00000399397.5:c.307T>G
|
ENSP00000382329.2:p.Phe103Val
|
|
ENST00000428619.1:c.124T>G
|
ENSP00000399057.2:p.Phe42Val
|
|
ENST00000498332.5:n.213T>G
|
|
|
NM_001277269.1:c.343T>G
|
NP_001264198.1:p.Phe115Val
|
|
NM_001292063.1:c.307T>G
|
NP_001278992.1:p.Phe103Val
|
|
NM_001277269.2:c.343T>G
|
NP_001264198.1:p.Phe115Val
|
|
NM_001292063.2:c.307T>G
MANE Select
|
NP_001278992.1:p.Phe103Val
|
|