ENST00000269980.7:c.654G>C
MANE Select
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ENSP00000269980.2:p.Gly218=
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ENST00000269980.6:c.654G>C
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ENSP00000269980.2:p.Gly218=
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ENST00000457836.6:c.588G>C
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ENSP00000416000.2:p.Gly196=
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ENST00000535632.5:n.283G>C
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ENST00000538423.5:n.780G>C
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ENST00000540732.3:c.756G>C
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ENSP00000443246.1:p.Gly252=
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ENST00000541315.1:c.554G>C
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ENST00000542943.5:c.567G>C
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ENSP00000440345.1:p.Gly189=
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ENST00000545787.1:n.282G>C
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ENST00000595085.5:c.654G>C
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ENSP00000471150.2:p.Gly218=
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NM_000709.3:c.654G>C
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NP_000700.1:p.Gly218=
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NM_001164783.1:c.654G>C
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NP_001158255.1:p.Gly218=
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NM_000709.4:c.654G>C
MANE Select
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NP_000700.1:p.Gly218=
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NM_001164783.2:c.654G>C
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NP_001158255.1:p.Gly218=
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