ENST00000350051.8:c.385G>T
MANE Select
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ENSP00000324180.4:p.Glu129Ter
|
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ENST00000301633.8:c.454G>T
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ENSP00000301633.3:p.Glu152Ter
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ENST00000350051.7:c.385G>T
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ENSP00000324180.4:p.Glu129Ter
|
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ENST00000374948.6:c.267G>T
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ENSP00000364086.1:p.Arg89=
|
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ENST00000589892.1:n.401G>T
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ENST00000590925.6:c.*187G>T
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ENSP00000467336.1:n.*187G>T
|
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NM_001012270.1:c.267G>T
|
NP_001012270.1:p.Arg89=
|
|
NM_001012271.1:c.454G>T
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NP_001012271.1:p.Glu152Ter
|
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NM_001168.2:c.385G>T
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NP_001159.2:p.Glu129Ter
|
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XR_243654.3:n.587G>T
|
|
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XR_934452.1:n.656G>T
|
|
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XR_243654.5:n.587G>T
|
|
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XR_934452.3:n.656G>T
|
|
|
NM_001168.3:c.385G>T
MANE Select
|
NP_001159.2:p.Glu129Ter
|
|
NM_001012270.2:c.267G>T
|
NP_001012270.1:p.Arg89=
|
|
NM_001012271.2:c.454G>T
|
NP_001012271.1:p.Glu152Ter
|
|