ENST00000378823.8:c.1805C>G
MANE Select
|
ENSP00000368100.4:p.Ala602Gly
|
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ENST00000638452.2:c.1508C>G
|
ENSP00000492349.2:p.Ala503Gly
|
|
ENST00000638504.1:n.1480-224C>G
|
|
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ENST00000638568.2:c.1508C>G
|
ENSP00000491158.2:p.Ala503Gly
|
|
ENST00000639899.1:n.2324C>G
|
|
|
ENST00000640655.2:c.1508C>G
|
ENSP00000491596.2:p.Ala503Gly
|
|
ENST00000651160.1:c.*16-224C>G
|
ENSP00000498829.1:n.*16-224C>G
|
|
ENST00000651658.1:n.2348C>G
|
|
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ENST00000651723.1:c.*1888C>G
|
ENSP00000498237.1:n.*1888C>G
|
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ENST00000652016.1:c.*88+203C>G
|
ENSP00000498267.1:n.*88+203C>G
|
|
ENST00000652485.1:c.1838C>G
|
ENSP00000498973.1:p.Ala613Gly
|
|
ENST00000378823.7:c.1805C>G
|
ENSP00000368100.4:p.Ala602Gly
|
|
ENST00000423956.5:c.1647C>G
|
ENSP00000390971.1:p.Ser549Arg
|
|
ENST00000453394.5:c.1622C>G
|
ENSP00000400049.1:p.Ala541Gly
|
|
ENST00000533482.5:c.*1431C>G
|
ENSP00000431225.1:n.*1431C>G
|
|
NM_005732.3:c.1805C>G
|
NP_005723.2:p.Ala602Gly
|
|
NM_005732.4:c.1805C>G
MANE Select
|
NP_005723.2:p.Ala602Gly
|
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