ENST00000350051.8:c.395G>A
MANE Select
|
ENSP00000324180.4:p.Arg132His
|
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ENST00000301633.8:c.464G>A
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ENSP00000301633.3:p.Arg155His
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|
ENST00000350051.7:c.395G>A
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ENSP00000324180.4:p.Arg132His
|
|
ENST00000374948.6:c.277G>A
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ENSP00000364086.1:p.Ala93Thr
|
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ENST00000589892.1:n.411G>A
|
|
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ENST00000590925.6:c.*197G>A
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ENSP00000467336.1:n.*197G>A
|
|
NM_001012270.1:c.277G>A
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NP_001012270.1:p.Ala93Thr
|
|
NM_001012271.1:c.464G>A
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NP_001012271.1:p.Arg155His
|
|
NM_001168.2:c.395G>A
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NP_001159.2:p.Arg132His
|
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XR_243654.3:n.597G>A
|
|
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XR_934452.1:n.666G>A
|
|
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XR_243654.5:n.597G>A
|
|
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XR_934452.3:n.666G>A
|
|
|
NM_001168.3:c.395G>A
MANE Select
|
NP_001159.2:p.Arg132His
|
|
NM_001012270.2:c.277G>A
|
NP_001012270.1:p.Ala93Thr
|
|
NM_001012271.2:c.464G>A
|
NP_001012271.1:p.Arg155His
|
|