ENST00000355265.7:c.617T>G
MANE Select
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ENSP00000347409.2:p.Phe206Cys
|
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ENST00000467543.6:c.*469T>G
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ENSP00000420011.2:n.*469T>G
|
|
ENST00000355265.6:c.617T>G
|
ENSP00000347409.2:p.Phe206Cys
|
|
ENST00000467543.5:c.560T>G
|
ENSP00000420011.1:p.Phe187Cys
|
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ENST00000476829.5:c.525+422T>G
|
ENSP00000419889.1:n.525+422T>G
|
|
ENST00000479768.6:n.735T>G
|
|
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ENST00000494148.1:n.216T>G
|
|
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NM_000420.2:c.617T>G
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NP_000411.1:p.Phe206Cys
|
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XM_005249993.2:c.653T>G
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XP_005250050.1:p.Phe218Cys
|
|
NM_000420.3:c.617T>G
MANE Select
|
NP_000411.1:p.Phe206Cys
|
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