ENST00000695651.1:n.2659C>A
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|
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ENST00000695653.1:c.2220C>A
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ENSP00000512084.1:p.Ala740=
|
|
ENST00000695654.1:c.3336C>A
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ENSP00000512085.1:p.Ala1112=
|
|
ENST00000695689.1:c.282C>A
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ENSP00000512101.1:n.282C>A
|
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ENST00000695690.1:n.502C>A
|
|
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ENST00000695691.1:n.502C>A
|
|
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ENST00000245907.11:c.4311C>A
MANE Select
|
ENSP00000245907.4:p.Ala1437=
|
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ENST00000245907.10:c.4311C>A
|
ENSP00000245907.4:p.Ala1437=
|
|
ENST00000596548.1:c.432C>A
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ENSP00000469744.1:p.Ala144=
|
|
ENST00000599899.5:n.1270C>A
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|
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ENST00000601008.1:c.242-4022C>A
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ENSP00000471384.1:n.242-4022C>A
|
|
NM_000064.3:c.4311C>A
|
NP_000055.2:p.Ala1437=
|
|
NM_000064.4:c.4311C>A
MANE Select
|
NP_000055.2:p.Ala1437=
|
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