ENST00000350051.8:c.420C>T
MANE Select
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ENSP00000324180.4:p.Ala140=
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ENST00000301633.8:c.489C>T
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ENSP00000301633.3:p.Ala163=
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ENST00000350051.7:c.420C>T
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ENSP00000324180.4:p.Ala140=
|
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ENST00000374948.6:c.302C>T
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ENSP00000364086.1:p.Pro101Leu
|
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ENST00000589892.1:n.436C>T
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|
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ENST00000590925.6:c.*222C>T
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ENSP00000467336.1:n.*222C>T
|
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NM_001012270.1:c.302C>T
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NP_001012270.1:p.Pro101Leu
|
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NM_001012271.1:c.489C>T
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NP_001012271.1:p.Ala163=
|
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NM_001168.2:c.420C>T
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NP_001159.2:p.Ala140=
|
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XR_243654.3:n.622C>T
|
|
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XR_934452.1:n.691C>T
|
|
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XR_243654.5:n.622C>T
|
|
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XR_934452.3:n.691C>T
|
|
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NM_001168.3:c.420C>T
MANE Select
|
NP_001159.2:p.Ala140=
|
|
NM_001012270.2:c.302C>T
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NP_001012270.1:p.Pro101Leu
|
|
NM_001012271.2:c.489C>T
|
NP_001012271.1:p.Ala163=
|
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