ENST00000542664.4:c.1340C>T
MANE Select
|
ENSP00000437737.1:p.Ala447Val
|
|
ENST00000543956.5:c.851C>T
|
ENSP00000441861.2:p.Ala284Val
|
|
ENST00000378688.8:c.1340C>T
|
ENSP00000367959.3:p.Ala447Val
|
|
ENST00000542664.3:c.1340C>T
|
ENSP00000437737.1:p.Ala447Val
|
|
ENST00000543956.4:c.1088C>T
|
ENSP00000441861.1:p.Ala363Val
|
|
NM_000621.4:c.1340C>T
|
NP_000612.1:p.Ala447Val
|
|
NM_001165947.2:c.1088C>T
|
NP_001159419.1:p.Ala363Val
|
|
NM_000621.5:c.1340C>T
MANE Select
|
NP_000612.1:p.Ala447Val
|
|
NM_001165947.5:c.851C>T
|
NP_001159419.2:p.Ala284Val
|
|
NM_001378924.1:c.1340C>T
|
NP_001365853.1:p.Ala447Val
|
|