ENST00000329841.10:c.221C>T
MANE Select
|
ENSP00000332256.5:p.Ala74Val
|
|
ENST00000329841.9:c.221C>T
|
ENSP00000332256.5:p.Ala74Val
|
|
ENST00000346623.6:c.221C>T
|
ENSP00000343294.6:p.Ala74Val
|
|
ENST00000558033.5:c.221C>T
|
ENSP00000454107.1:p.Ala74Val
|
|
ENST00000560555.1:n.281C>T
|
|
|
ENST00000561338.5:c.137C>T
|
ENSP00000452789.1:p.Ala46Val
|
|
NM_000693.3:c.221C>T
|
NP_000684.2:p.Ala74Val
|
|
NM_001293815.1:c.221C>T
|
NP_001280744.1:p.Ala74Val
|
|
NM_000693.4:c.221C>T
MANE Select
|
NP_000684.2:p.Ala74Val
|
|
NM_001293815.2:c.221C>T
|
NP_001280744.1:p.Ala74Val
|
|