ENST00000297289.9:c.982A>G
|
ENSP00000516619.1:p.Ile328Val
|
|
ENST00000418964.2:c.2080A>G
|
ENSP00000389424.2:p.Ile694Val
|
|
ENST00000706906.1:c.*2049A>G
|
ENSP00000516618.1:n.*2049A>G
|
|
ENST00000308192.14:c.2029A>G
MANE Select
|
ENSP00000308938.9:p.Ile677Val
|
|
ENST00000308192.13:c.2029A>G
|
ENSP00000308938.9:p.Ile677Val
|
|
ENST00000461414.2:n.52A>G
|
|
|
ENST00000467466.1:n.330A>G
|
|
|
NM_000301.3:c.2029A>G , LRG_571t1:c.2029A>G
|
NP_000292.1:p.Ile677Val
|
|
NM_000301.4:c.2029A>G
|
NP_000292.1:p.Ile677Val
|
|
NM_000301.5:c.2029A>G
MANE Select
|
NP_000292.1:p.Ile677Val
|
|