ENST00000302068.9:c.1228A>G
MANE Select
|
ENSP00000306099.4:p.Arg410Gly
|
|
ENST00000302068.8:c.1228A>G
|
ENSP00000306099.4:p.Arg410Gly
|
|
ENST00000502545.5:n.939+476A>G
|
|
|
ENST00000509493.1:c.571A>G
|
ENSP00000426757.1:p.Arg191Gly
|
|
NM_001184741.1:c.1051A>G
|
NP_001171670.1:p.Arg351Gly
|
|
NM_005141.4:c.1228A>G , LRG_558t1:c.1228A>G
|
NP_005132.2:p.Arg410Gly
|
|
NM_001382759.1:c.1096A>G
|
NP_001369688.1:p.Arg366Gly
|
|
NM_001382760.1:c.1228A>G
|
NP_001369689.1:p.Arg410Gly
|
|
NM_001382761.1:c.1228A>G
|
NP_001369690.1:p.Arg410Gly
|
|
NM_001382762.1:c.928A>G
|
NP_001369691.1:p.Arg310Gly
|
|
NM_001382763.1:c.1219A>G
|
NP_001369692.1:p.Arg407Gly
|
|
NM_001382764.1:c.*2A>G
|
NP_001369693.1:n.*2A>G
|
|
NM_001382765.1:c.1220+8A>G
|
NP_001369694.1:n.1220+8A>G
|
|
NM_005141.5:c.1228A>G
MANE Select
|
NP_005132.2:p.Arg410Gly
|
|