ENST00000295408.9:c.1510A>G
MANE Select
|
ENSP00000295408.4:p.Ile504Val
|
|
ENST00000295408.8:c.1510A>G
|
ENSP00000295408.4:p.Ile504Val
|
|
ENST00000409780.5:c.982A>G
|
ENSP00000387277.1:p.Ile328Val
|
|
ENST00000421804.6:c.1510A>G
|
ENSP00000389152.2:p.Ile504Val
|
|
ENST00000439966.5:c.*983A>G
|
ENSP00000402129.1:n.*983A>G
|
|
ENST00000473065.1:n.13A>G
|
|
|
ENST00000616902.4:c.479A>G
|
ENSP00000482824.1:p.His160Arg
|
|
NM_006343.2:c.1510A>G
|
NP_006334.2:p.Ile504Val
|
|
XM_005263565.3:c.1510A>G
|
XP_005263622.1:p.Ile504Val
|
|
XM_005263568.3:c.1510A>G
|
XP_005263625.1:p.Ile504Val
|
|
XM_011510490.1:c.1321A>G
|
XP_011508792.1:p.Ile441Val
|
|
XM_011510491.1:c.295A>G
|
XP_011508793.1:p.Ile99Val
|
|
XM_005263565.4:c.1510A>G
|
XP_005263622.1:p.Ile504Val
|
|
XM_005263568.4:c.1510A>G
|
XP_005263625.1:p.Ile504Val
|
|
XM_011510490.3:c.1321A>G
|
XP_011508792.1:p.Ile441Val
|
|
XM_017003164.1:c.1321A>G
|
XP_016858653.1:p.Ile441Val
|
|
XM_017003165.2:c.295A>G
|
XP_016858654.1:p.Ile99Val
|
|
NM_006343.3:c.1510A>G
MANE Select
|
NP_006334.2:p.Ile504Val
|
|