ENST00000264381.8:c.1730G>A
MANE Select
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ENSP00000264381.3:p.Arg577His
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ENST00000264381.7:c.1730G>A
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ENSP00000264381.3:p.Arg577His
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ENST00000479451.5:c.320G>A
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ENSP00000418325.1:p.Arg107His
|
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ENST00000482958.1:c.*236G>A
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ENSP00000419804.1:n.*236G>A
|
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ENST00000497011.5:c.*120G>A
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ENSP00000419505.1:n.*120G>A
|
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NM_000055.2:c.1730G>A
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NP_000046.1:p.Arg577His
|
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XM_005247685.1:c.1853G>A
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XP_005247742.1:p.Arg618His
|
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NM_000055.3:c.1730G>A
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NP_000046.1:p.Arg577His
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NR_137635.1:n.372G>A
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NR_137636.1:n.1976G>A
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|
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NM_000055.4:c.1730G>A
MANE Select
|
NP_000046.1:p.Arg577His
|
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NR_137635.2:n.323G>A
|
|
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NR_137636.2:n.1927G>A
|
|
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