ENST00000350051.8:c.390A>G
MANE Select
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ENSP00000324180.4:p.Lys130=
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ENST00000301633.8:c.459A>G
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ENSP00000301633.3:p.Lys153=
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ENST00000350051.7:c.390A>G
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ENSP00000324180.4:p.Lys130=
|
|
ENST00000374948.6:c.272A>G
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ENSP00000364086.1:p.Lys91Arg
|
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ENST00000589892.1:n.406A>G
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|
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ENST00000590925.6:c.*192A>G
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ENSP00000467336.1:n.*192A>G
|
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NM_001012270.1:c.272A>G
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NP_001012270.1:p.Lys91Arg
|
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NM_001012271.1:c.459A>G
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NP_001012271.1:p.Lys153=
|
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NM_001168.2:c.390A>G
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NP_001159.2:p.Lys130=
|
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XR_243654.3:n.592A>G
|
|
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XR_934452.1:n.661A>G
|
|
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XR_243654.5:n.592A>G
|
|
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XR_934452.3:n.661A>G
|
|
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NM_001168.3:c.390A>G
MANE Select
|
NP_001159.2:p.Lys130=
|
|
NM_001012270.2:c.272A>G
|
NP_001012270.1:p.Lys91Arg
|
|
NM_001012271.2:c.459A>G
|
NP_001012271.1:p.Lys153=
|
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