ENST00000354177.9:c.650C>T
|
ENSP00000346109.5:p.Ala217Val
|
|
ENST00000494537.2:c.719C>T
|
ENSP00000508308.1:p.Ala240Val
|
|
ENST00000361547.7:c.821C>T
MANE Select
|
ENSP00000355141.2:p.Ala274Val
|
|
ENST00000354177.8:c.719C>T
|
ENSP00000346109.4:p.Ala240Val
|
|
ENST00000361547.6:c.821C>T
|
ENSP00000355141.2:p.Ala274Val
|
|
ENST00000374315.1:c.719C>T
|
ENSP00000363434.1:p.Ala240Val
|
|
NM_020451.2:c.821C>T
|
NP_065184.2:p.Ala274Val
|
|
NM_206926.1:c.719C>T
|
NP_996809.1:p.Ala240Val
|
|
NM_020451.3:c.821C>T
MANE Select
|
NP_065184.2:p.Ala274Val
|
|
NM_206926.2:c.719C>T
|
NP_996809.1:p.Ala240Val
|
|