ENST00000295408.9:c.685A>G
MANE Select
|
ENSP00000295408.4:p.Ile229Val
|
|
ENST00000295408.8:c.685A>G
|
ENSP00000295408.4:p.Ile229Val
|
|
ENST00000409780.5:c.157A>G
|
ENSP00000387277.1:p.Ile53Val
|
|
ENST00000421804.6:c.685A>G
|
ENSP00000389152.2:p.Ile229Val
|
|
ENST00000439966.5:c.*158A>G
|
ENSP00000402129.1:n.*158A>G
|
|
ENST00000616902.4:c.-531A>G
|
ENSP00000482824.1:n.-531A>G
|
|
NM_006343.2:c.685A>G
|
NP_006334.2:p.Ile229Val
|
|
XM_005263565.3:c.685A>G
|
XP_005263622.1:p.Ile229Val
|
|
XM_005263568.3:c.685A>G
|
XP_005263625.1:p.Ile229Val
|
|
XM_011510490.1:c.496A>G
|
XP_011508792.1:p.Ile166Val
|
|
XM_005263565.4:c.685A>G
|
XP_005263622.1:p.Ile229Val
|
|
XM_005263568.4:c.685A>G
|
XP_005263625.1:p.Ile229Val
|
|
XM_011510490.3:c.496A>G
|
XP_011508792.1:p.Ile166Val
|
|
XM_017003164.1:c.496A>G
|
XP_016858653.1:p.Ile166Val
|
|
XM_017003165.2:c.-583A>G
|
XP_016858654.1:n.-583A>G
|
|
NM_006343.3:c.685A>G
MANE Select
|
NP_006334.2:p.Ile229Val
|
|