ENST00000261647.10:c.86T>A
MANE Select
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ENSP00000261647.5:p.Leu29His
|
|
ENST00000261647.9:c.86T>A
|
ENSP00000261647.5:p.Leu29His
|
|
ENST00000466729.5:c.151T>A
|
|
|
ENST00000470399.1:c.101T>A
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ENSP00000465082.1:p.Leu34His
|
|
ENST00000475723.5:c.133T>A
|
|
|
ENST00000497842.6:n.111T>A
|
|
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ENST00000583704.1:n.111T>A
|
|
|
NM_001271420.1:c.-373T>A
|
NP_001258349.1:n.-373T>A
|
|
NM_017775.3:c.86T>A
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NP_060245.3:p.Leu29His
|
|
XM_011523950.1:c.86T>A
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XP_011522252.1:p.Leu29His
|
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XM_017024801.2:c.86T>A
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XP_016880290.2:p.Leu29His
|
|
XM_017024802.2:c.86T>A
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XP_016880291.2:p.Leu29His
|
|
XM_024450814.1:c.86T>A
|
XP_024306582.1:p.Leu29His
|
|
NM_017775.4:c.86T>A
MANE Select
|
NP_060245.3:p.Leu29His
|
|
NM_001271420.2:c.-373T>A
|
NP_001258349.1:n.-373T>A
|
|