ENST00000255030.9:c.584G>T
MANE Select
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ENSP00000255030.5:p.Gly195Val
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ENST00000368110.1:c.218G>T
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ENSP00000357091.1:p.Gly73Val
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ENST00000368111.5:c.218G>T
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ENSP00000357092.1:p.Gly73Val
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ENST00000368112.5:c.198-13G>T
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ENSP00000357093.1:n.198-13G>T
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ENST00000437342.1:c.50G>T
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ENSP00000402788.1:p.Gly17Val
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ENST00000473196.1:n.152G>T
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ENST00000489317.1:n.74+391G>T
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NM_000567.2:c.584G>T
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NP_000558.2:p.Gly195Val
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XM_011509207.1:c.584G>T
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XP_011507509.1:p.Gly195Val
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NM_001329057.1:c.584G>T
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NP_001315986.1:p.Gly195Val
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NM_001329058.1:c.198-13G>T
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NP_001315987.1:n.198-13G>T
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NM_000567.3:c.584G>T
MANE Select
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NP_000558.2:p.Gly195Val
|
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NM_001329057.2:c.584G>T
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NP_001315986.1:p.Gly195Val
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NM_001329058.2:c.198-13G>T
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NP_001315987.1:n.198-13G>T
|
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NM_001382703.1:c.218G>T
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NP_001369632.1:p.Gly73Val
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