ENST00000270357.10:c.1582A>C
MANE Select
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ENSP00000270357.4:p.Ser528Arg
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ENST00000270357.8:c.889A>C
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ENSP00000270357.3:p.Ser297Arg
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ENST00000437406.1:c.148A>C
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ENSP00000403319.1:p.Ser50Arg
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ENST00000451363.5:c.223A>C
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ENSP00000414661.1:p.Ser75Arg
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ENST00000464550.5:n.418A>C
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ENST00000471657.1:n.385A>C
|
|
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ENST00000481757.5:n.2516A>C
|
|
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ENST00000486058.5:n.1695A>C
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|
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ENST00000493398.5:n.728A>C
|
|
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NM_018226.4:c.1582A>C
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NP_060696.4:p.Ser528Arg
|
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XM_005247036.3:c.1549A>C
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XP_005247093.1:p.Ser517Arg
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NM_018226.5:c.1582A>C
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NP_060696.4:p.Ser528Arg
|
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XM_005247036.4:c.1549A>C
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XP_005247093.1:p.Ser517Arg
|
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NM_018226.6:c.1582A>C
MANE Select
|
NP_060696.4:p.Ser528Arg
|
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