ENST00000290866.10:c.2372G=
MANE Select
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ENSP00000290866.4:p.Arg791=
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|
ENST00000290863.10:c.650G=
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ENSP00000290863.6:p.Arg217=
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ENST00000290866.9:c.2372G=
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ENSP00000290866.4:p.Arg791=
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ENST00000413513.7:c.650G=
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ENSP00000392247.3:p.Arg217=
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ENST00000428043.5:c.2372G=
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ENSP00000397593.2:p.Arg791=
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|
ENST00000577647.2:c.650G=
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ENSP00000464149.1:p.Arg217=
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ENST00000578839.5:c.*442G=
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ENSP00000462110.2:n.*442G=
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|
ENST00000579204.1:c.631G=
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ENSP00000464629.1:n.631G=
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|
ENST00000579314.5:c.*101G=
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ENSP00000462599.1:n.*101G=
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|
ENST00000582005.5:c.*292G=
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ENSP00000462002.1:n.*292G=
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|
ENST00000582761.1:c.140G=
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ENSP00000462909.1:p.Arg47=
|
|
ENST00000584865.5:n.318G=
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|
|
NM_000789.3:c.2372G=
|
NP_000780.1:p.Arg791=
|
|
NM_001178057.1:c.650G=
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NP_001171528.1:p.Arg217=
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|
NM_152830.2:c.650G=
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NP_690043.1:p.Arg217=
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|
XM_005257110.1:c.1823G=
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XP_005257167.1:p.Arg608=
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|
XM_006721737.2:c.710G=
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XP_006721800.2:p.Arg237=
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|
XM_006721737.3:c.710G=
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XP_006721800.2:p.Arg237=
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|
NM_000789.4:c.2372G=
MANE Select
|
NP_000780.1:p.Arg791=
|
|
NM_001178057.2:c.650G=
|
NP_001171528.1:p.Arg217=
|
|
NM_152830.3:c.650G=
|
NP_690043.1:p.Arg217=
|
|
NM_001382700.1:c.1805G=
|
NP_001369629.1:p.Arg602=
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|
NM_001382701.1:c.1520G=
|
NP_001369630.1:p.Arg507=
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|
NM_001382702.1:c.302G=
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NP_001369631.1:p.Arg101=
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NR_168483.1:n.750G=
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|
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