ENST00000375820.10:c.328A>G
MANE Select
|
ENSP00000364979.4:p.Ile110Val
|
|
ENST00000543140.6:c.328A>G
|
ENSP00000443348.1:p.Ile110Val
|
|
ENST00000615732.2:c.136A>G
|
ENSP00000478222.2:p.Ile46Val
|
|
ENST00000647797.1:c.207A>G
|
|
|
ENST00000648170.1:n.207A>G
|
|
|
ENST00000648966.1:c.207A>G
|
|
|
ENST00000649484.1:c.207A>G
|
|
|
ENST00000649738.1:n.458A>G
|
|
|
ENST00000650138.1:n.17A>G
|
|
|
ENST00000375820.8:c.328A>G
|
ENSP00000364979.4:p.Ile110Val
|
|
ENST00000543140.5:c.328A>G
|
ENSP00000443348.1:p.Ile110Val
|
|
ENST00000615732.1:c.136A>G
|
ENSP00000478222.1:p.Ile46Val
|
|
NM_001303110.1:c.328A>G
|
NP_001290039.1:p.Ile110Val
|
|
NM_001845.5:c.328A>G
|
NP_001836.3:p.Ile110Val
|
|
XM_011521048.1:c.136A>G
|
XP_011519350.1:p.Ile46Val
|
|
XM_011521048.2:c.136A>G
|
XP_011519350.1:p.Ile46Val
|
|
NM_001845.6:c.328A>G
MANE Select
|
NP_001836.3:p.Ile110Val
|
|
NM_001303110.2:c.328A>G
|
NP_001290039.1:p.Ile110Val
|
|