ENST00000355832.10:c.2141G>T
MANE Select
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ENSP00000348089.5:p.Gly714Val
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ENST00000681632.1:n.2219G>T
|
|
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ENST00000681659.1:c.1982G>T
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ENSP00000505631.1:p.Gly661Val
|
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ENST00000355832.9:c.2141G>T
|
ENSP00000348089.5:p.Gly714Val
|
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ENST00000623073.3:c.*533G>T
|
ENSP00000485650.1:n.*533G>T
|
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ENST00000623115.3:c.251G>T
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ENSP00000485321.1:p.Gly84Val
|
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NM_000124.3:c.2141G>T
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NP_000115.1:p.Gly714Val
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NM_001346440.1:c.2141G>T
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NP_001333369.1:p.Gly714Val
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NM_000124.4:c.2141G>T
MANE Select
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NP_000115.1:p.Gly714Val
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NM_001346440.2:c.2141G>T
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NP_001333369.1:p.Gly714Val
|
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