ENST00000356839.10:c.1364T>A
MANE Select
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ENSP00000349297.5:p.Leu455His
|
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ENST00000322910.9:c.*1319T>A
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ENSP00000325395.5:n.*1319T>A
|
|
ENST00000350303.9:c.1298T>A
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ENSP00000344152.5:p.Leu433His
|
|
ENST00000356839.9:c.1364T>A
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ENSP00000349297.5:p.Leu455His
|
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ENST00000542255.6:c.222T>A
|
|
|
ENST00000543245.6:c.1433T>A
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ENSP00000438689.2:p.Leu478His
|
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ENST00000578711.1:n.495T>A
|
|
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ENST00000579425.5:n.480T>A
|
|
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ENST00000579546.1:c.201T>A
|
|
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ENST00000579894.5:n.75T>A
|
|
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ENST00000583074.5:n.83T>A
|
|
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ENST00000583850.5:n.139T>A
|
|
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ENST00000583858.5:c.393T>A
|
|
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ENST00000585203.6:n.555T>A
|
|
|
NM_000018.3:c.1364T>A
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NP_000009.1:p.Leu455His
|
|
NM_001033859.2:c.1298T>A
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NP_001029031.1:p.Leu433His
|
|
NM_001270447.1:c.1433T>A
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NP_001257376.1:p.Leu478His
|
|
NM_001270448.1:c.1136T>A
|
NP_001257377.1:p.Leu379His
|
|
XM_006721516.2:c.1364T>A
|
XP_006721579.2:p.Leu455His
|
|
XM_011523829.1:c.1364T>A
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XP_011522131.1:p.Leu455His
|
|
XM_011523830.1:c.1364T>A
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XP_011522132.1:p.Leu455His
|
|
XR_934021.1:n.1471T>A
|
|
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XR_934022.1:n.1471T>A
|
|
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XR_934023.1:n.1471T>A
|
|
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XM_006721516.3:c.1364T>A
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XP_006721579.2:p.Leu455His
|
|
XM_011523829.2:c.1364T>A
|
XP_011522131.1:p.Leu455His
|
|
XM_011523830.2:c.1364T>A
|
XP_011522132.1:p.Leu455His
|
|
XM_024450741.1:c.1364T>A
|
XP_024306509.1:p.Leu455His
|
|
XR_934021.2:n.1423T>A
|
|
|
XR_934022.2:n.1423T>A
|
|
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XR_934023.2:n.1423T>A
|
|
|
NM_000018.4:c.1364T>A
MANE Select
|
NP_000009.1:p.Leu455His
|
|
NM_001033859.3:c.1298T>A
|
NP_001029031.1:p.Leu433His
|
|
NM_001270447.2:c.1433T>A
|
NP_001257376.1:p.Leu478His
|
|
NM_001270448.2:c.1136T>A
|
NP_001257377.1:p.Leu379His
|
|