ENST00000396705.10:c.741C>A
MANE Select
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ENSP00000379933.4:p.Ala247=
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ENST00000229270.8:c.852C>A
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ENSP00000229270.4:p.Ala284=
|
|
ENST00000396705.9:c.741C>A
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ENSP00000379933.4:p.Ala247=
|
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ENST00000474253.1:n.230C>A
|
|
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ENST00000488464.6:c.495C>A
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ENSP00000475620.1:p.Ala165=
|
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ENST00000535434.5:c.495C>A
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ENSP00000443599.1:p.Ala165=
|
|
ENST00000613953.4:c.852C>A
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ENSP00000484435.1:p.Ala284=
|
|
NM_000365.5:c.741C>A
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NP_000356.1:p.Ala247=
|
|
NM_001159287.1:c.852C>A
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NP_001152759.1:p.Ala284=
|
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NM_001258026.1:c.495C>A
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NP_001244955.1:p.Ala165=
|
|
XR_002957378.1:n.1749C>A
|
|
|
NM_000365.6:c.741C>A
MANE Select
|
NP_000356.1:p.Ala247=
|
|
NM_001258026.2:c.495C>A
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NP_001244955.1:p.Ala165=
|
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