ENST00000354177.9:c.656C>T
|
ENSP00000346109.5:p.Ala219Val
|
|
ENST00000494537.2:c.725C>T
|
ENSP00000508308.1:p.Ala242Val
|
|
ENST00000361547.7:c.827C>T
MANE Select
|
ENSP00000355141.2:p.Ala276Val
|
|
ENST00000354177.8:c.725C>T
|
ENSP00000346109.4:p.Ala242Val
|
|
ENST00000361547.6:c.827C>T
|
ENSP00000355141.2:p.Ala276Val
|
|
ENST00000374315.1:c.725C>T
|
ENSP00000363434.1:p.Ala242Val
|
|
NM_020451.2:c.827C>T
|
NP_065184.2:p.Ala276Val
|
|
NM_206926.1:c.725C>T
|
NP_996809.1:p.Ala242Val
|
|
NM_020451.3:c.827C>T
MANE Select
|
NP_065184.2:p.Ala276Val
|
|
NM_206926.2:c.725C>T
|
NP_996809.1:p.Ala242Val
|
|