ENST00000295408.9:c.343T>G
MANE Select
|
ENSP00000295408.4:p.Cys115Gly
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|
ENST00000295408.8:c.343T>G
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ENSP00000295408.4:p.Cys115Gly
|
|
ENST00000409780.5:c.-46-15559T>G
|
ENSP00000387277.1:n.-46-15559T>G
|
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ENST00000421804.6:c.343T>G
|
ENSP00000389152.2:p.Cys115Gly
|
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ENST00000439966.5:c.246+97T>G
|
ENSP00000402129.1:n.246+97T>G
|
|
ENST00000616902.4:c.-873T>G
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ENSP00000482824.1:n.-873T>G
|
|
NM_006343.2:c.343T>G
|
NP_006334.2:p.Cys115Gly
|
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XM_005263565.3:c.343T>G
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XP_005263622.1:p.Cys115Gly
|
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XM_005263568.3:c.343T>G
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XP_005263625.1:p.Cys115Gly
|
|
XM_011510490.1:c.154T>G
|
XP_011508792.1:p.Cys52Gly
|
|
XM_005263565.4:c.343T>G
|
XP_005263622.1:p.Cys115Gly
|
|
XM_005263568.4:c.343T>G
|
XP_005263625.1:p.Cys115Gly
|
|
XM_011510490.3:c.154T>G
|
XP_011508792.1:p.Cys52Gly
|
|
XM_017003164.1:c.154T>G
|
XP_016858653.1:p.Cys52Gly
|
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XM_017003165.2:c.-925T>G
|
XP_016858654.1:n.-925T>G
|
|
NM_006343.3:c.343T>G
MANE Select
|
NP_006334.2:p.Cys115Gly
|
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