ENST00000426263.10:c.992C>G
MANE Select
|
ENSP00000416293.2:p.Ala331Gly
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ENST00000674545.1:n.486C>G
|
|
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ENST00000674765.1:c.992C>G
|
ENSP00000501811.1:p.Ala331Gly
|
|
ENST00000675112.1:n.1293C>G
|
|
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ENST00000676254.1:n.1441C>G
|
|
|
ENST00000426263.7:c.992C>G
|
ENSP00000416293.2:p.Ala331Gly
|
|
ENST00000475162.3:c.415+1612C>G
|
|
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ENST00000630287.2:c.*307C>G
|
ENSP00000486694.1:n.*307C>G
|
|
NM_006516.2:c.992C>G
|
NP_006507.2:p.Ala331Gly
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NM_006516.3:c.992C>G
|
NP_006507.2:p.Ala331Gly
|
|
NM_006516.4:c.992C>G
MANE Select
|
NP_006507.2:p.Ala331Gly
|
|