ENST00000359842.10:c.412A>G
MANE Select
|
ENSP00000352900.5:p.Ile138Val
|
|
ENST00000359842.9:c.412A>G
|
ENSP00000352900.5:p.Ile138Val
|
|
ENST00000470566.1:n.337A>G
|
|
|
ENST00000619224.1:c.43A>G
|
ENSP00000482458.1:p.Ile15Val
|
|
NM_001256570.1:c.43A>G
|
NP_001243499.1:p.Ile15Val
|
|
NM_001256571.1:c.43A>G
|
NP_001243500.1:p.Ile15Val
|
|
NM_006917.4:c.412A>G
|
NP_008848.1:p.Ile138Val
|
|
NM_006917.5:c.412A>G
MANE Select
|
NP_008848.1:p.Ile138Val
|
|
NM_001256571.2:c.43A>G
|
NP_001243500.1:p.Ile15Val
|
|
NM_001256570.2:c.43A>G
|
NP_001243499.1:p.Ile15Val
|
|