ENST00000338034.9:c.2342G>A
MANE Select
|
ENSP00000337445.4:p.Arg781His
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ENST00000338034.8:c.2342G>A
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ENSP00000337445.4:p.Arg781His
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ENST00000395962.6:c.2285G>A
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ENSP00000379291.1:p.Arg762His
|
|
ENST00000426905.7:c.2222G>A
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ENSP00000405223.3:p.Arg741His
|
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ENST00000465825.5:n.2229G>A
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|
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ENST00000480891.5:n.2171G>A
|
|
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ENST00000484122.5:n.3172G>A
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|
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ENST00000487229.6:n.1888G>A
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|
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ENST00000584650.5:c.1741G>A
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|
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NM_001165962.1:c.2222G>A
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NP_001159434.1:p.Arg741His
|
|
NM_018127.6:c.2342G>A
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NP_060597.4:p.Arg781His
|
|
NM_173717.1:c.2339G>A
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NP_776065.1:p.Arg780His
|
|
XM_024450850.1:c.2501G>A
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XP_024306618.1:p.Arg834His
|
|
XM_024450851.1:c.2423G>A
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XP_024306619.1:p.Arg808His
|
|
XM_024450852.1:c.2420G>A
|
XP_024306620.1:p.Arg807His
|
|
XM_024450853.1:c.2417G>A
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XP_024306621.1:p.Arg806His
|
|
XM_024450854.1:c.2381G>A
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XP_024306622.1:p.Arg794His
|
|
XM_024450855.1:c.2300G>A
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XP_024306623.1:p.Arg767His
|
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XM_024450856.1:c.2219G>A
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XP_024306624.1:p.Arg740His
|
|
XM_024450857.1:c.2219G>A
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XP_024306625.1:p.Arg740His
|
|
XM_024450858.1:c.2138G>A
|
XP_024306626.1:p.Arg713His
|
|
XM_024450859.1:c.2135G>A
|
XP_024306627.1:p.Arg712His
|
|
XM_024450860.1:c.2060G>A
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XP_024306628.1:p.Arg687His
|
|
XM_024450861.1:c.2060G>A
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XP_024306629.1:p.Arg687His
|
|
XM_024450862.1:c.2057G>A
|
XP_024306630.1:p.Arg686His
|
|
NM_018127.7:c.2342G>A
MANE Select
|
NP_060597.4:p.Arg781His
|
|
NM_001165962.2:c.2222G>A
|
NP_001159434.1:p.Arg741His
|
|
NM_173717.2:c.2339G>A
|
NP_776065.1:p.Arg780His
|
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