ENST00000295408.9:c.1586T>G
MANE Select
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ENSP00000295408.4:p.Val529Gly
|
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ENST00000295408.8:c.1586T>G
|
ENSP00000295408.4:p.Val529Gly
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|
ENST00000409780.5:c.1058T>G
|
ENSP00000387277.1:p.Val353Gly
|
|
ENST00000421804.6:c.1586T>G
|
ENSP00000389152.2:p.Val529Gly
|
|
ENST00000439966.5:c.*1059T>G
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ENSP00000402129.1:n.*1059T>G
|
|
ENST00000473065.1:n.89T>G
|
|
|
ENST00000616902.4:c.551T>G
|
ENSP00000482824.1:p.Val184Gly
|
|
NM_006343.2:c.1586T>G
|
NP_006334.2:p.Val529Gly
|
|
XM_005263565.3:c.1586T>G
|
XP_005263622.1:p.Val529Gly
|
|
XM_005263568.3:c.1586T>G
|
XP_005263625.1:p.Val529Gly
|
|
XM_011510490.1:c.1397T>G
|
XP_011508792.1:p.Val466Gly
|
|
XM_011510491.1:c.371T>G
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XP_011508793.1:p.Val124Gly
|
|
XM_005263565.4:c.1586T>G
|
XP_005263622.1:p.Val529Gly
|
|
XM_005263568.4:c.1586T>G
|
XP_005263625.1:p.Val529Gly
|
|
XM_011510490.3:c.1397T>G
|
XP_011508792.1:p.Val466Gly
|
|
XM_017003164.1:c.1397T>G
|
XP_016858653.1:p.Val466Gly
|
|
XM_017003165.2:c.371T>G
|
XP_016858654.1:p.Val124Gly
|
|
NM_006343.3:c.1586T>G
MANE Select
|
NP_006334.2:p.Val529Gly
|
|