ENST00000481739.2:c.319A>G
MANE Select
|
ENSP00000419692.1:p.Ile107Val
|
|
ENST00000672570.1:c.238A>G
|
ENSP00000500402.1:p.Ile80Val
|
|
ENST00000356384.4:n.729A>G
|
|
|
ENST00000481739.1:c.319A>G
|
ENSP00000419692.1:p.Ile107Val
|
|
NM_001291920.1:c.238A>G
|
NP_001278849.1:p.Ile80Val
|
|
NM_001291921.1:c.28A>G
|
NP_001278850.1:p.Ile10Val
|
|
NM_002957.5:c.319A>G
|
NP_002948.1:p.Ile107Val
|
|
NM_002957.6:c.319A>G
MANE Select
|
NP_002948.1:p.Ile107Val
|
|
NM_001291921.2:c.28A>G
|
NP_001278850.1:p.Ile10Val
|
|
NM_001291920.2:c.238A>G
|
NP_001278849.1:p.Ile80Val
|
|