ENST00000338034.9:c.2390G>A
MANE Select
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ENSP00000337445.4:p.Arg797Lys
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ENST00000338034.8:c.2390G>A
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ENSP00000337445.4:p.Arg797Lys
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ENST00000395962.6:c.2333G>A
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ENSP00000379291.1:p.Arg778Lys
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|
ENST00000426905.7:c.2270G>A
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ENSP00000405223.3:p.Arg757Lys
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ENST00000465825.5:n.2277G>A
|
|
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ENST00000480891.5:n.2219G>A
|
|
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ENST00000484122.5:n.3220G>A
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|
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ENST00000487229.6:n.1936G>A
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|
|
ENST00000584650.5:c.1789G>A
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|
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NM_001165962.1:c.2270G>A
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NP_001159434.1:p.Arg757Lys
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NM_018127.6:c.2390G>A
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NP_060597.4:p.Arg797Lys
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|
NM_173717.1:c.2387G>A
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NP_776065.1:p.Arg796Lys
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|
XM_024450850.1:c.2549G>A
|
XP_024306618.1:p.Arg850Lys
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|
XM_024450851.1:c.2471G>A
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XP_024306619.1:p.Arg824Lys
|
|
XM_024450852.1:c.2468G>A
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XP_024306620.1:p.Arg823Lys
|
|
XM_024450853.1:c.2465G>A
|
XP_024306621.1:p.Arg822Lys
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|
XM_024450854.1:c.2429G>A
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XP_024306622.1:p.Arg810Lys
|
|
XM_024450855.1:c.2348G>A
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XP_024306623.1:p.Arg783Lys
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|
XM_024450856.1:c.2267G>A
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XP_024306624.1:p.Arg756Lys
|
|
XM_024450857.1:c.2267G>A
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XP_024306625.1:p.Arg756Lys
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|
XM_024450858.1:c.2186G>A
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XP_024306626.1:p.Arg729Lys
|
|
XM_024450859.1:c.2183G>A
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XP_024306627.1:p.Arg728Lys
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|
XM_024450860.1:c.2108G>A
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XP_024306628.1:p.Arg703Lys
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|
XM_024450861.1:c.2108G>A
|
XP_024306629.1:p.Arg703Lys
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|
XM_024450862.1:c.2105G>A
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XP_024306630.1:p.Arg702Lys
|
|
NM_018127.7:c.2390G>A
MANE Select
|
NP_060597.4:p.Arg797Lys
|
|
NM_001165962.2:c.2270G>A
|
NP_001159434.1:p.Arg757Lys
|
|
NM_173717.2:c.2387G>A
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NP_776065.1:p.Arg796Lys
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