ENST00000270357.10:c.1554G>A
MANE Select
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ENSP00000270357.4:p.Leu518=
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ENST00000270357.8:c.861G>A
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ENSP00000270357.3:p.Leu287=
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ENST00000437406.1:c.120G>A
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ENSP00000403319.1:p.Leu40=
|
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ENST00000451363.5:c.195G>A
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ENSP00000414661.1:p.Leu65=
|
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ENST00000464550.5:n.390G>A
|
|
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ENST00000471657.1:n.357G>A
|
|
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ENST00000481757.5:n.2488G>A
|
|
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ENST00000486058.5:n.1667G>A
|
|
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ENST00000493398.5:n.700G>A
|
|
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NM_018226.4:c.1554G>A
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NP_060696.4:p.Leu518=
|
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XM_005247036.3:c.1521G>A
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XP_005247093.1:p.Leu507=
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NM_018226.5:c.1554G>A
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NP_060696.4:p.Leu518=
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|
XM_005247036.4:c.1521G>A
|
XP_005247093.1:p.Leu507=
|
|
NM_018226.6:c.1554G>A
MANE Select
|
NP_060696.4:p.Leu518=
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