ENST00000268125.10:c.583A>G
MANE Select
|
ENSP00000268125.5:p.Ile195Val
|
|
ENST00000268125.9:c.583A>G
|
ENSP00000268125.5:p.Ile195Val
|
|
ENST00000567787.1:c.*161A>G
|
ENSP00000457251.1:n.*161A>G
|
|
NM_000326.4:c.583A>G
|
NP_000317.1:p.Ile195Val
|
|
XM_011521870.1:c.583A>G
|
XP_011520172.1:p.Ile195Val
|
|
XM_011521871.1:c.508A>G
|
XP_011520173.1:p.Ile170Val
|
|
XM_011521872.1:c.508A>G
|
XP_011520174.1:p.Ile170Val
|
|
XM_011521870.2:c.583A>G
|
XP_011520172.1:p.Ile195Val
|
|
XM_017022460.1:c.610A>G
|
XP_016877949.1:p.Ile204Val
|
|
NM_000326.5:c.583A>G
MANE Select
|
NP_000317.1:p.Ile195Val
|
|