ENST00000290866.10:c.351G>A
MANE Select
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ENSP00000290866.4:p.Leu117=
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ENST00000290866.9:c.351G>A
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ENSP00000290866.4:p.Leu117=
|
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ENST00000428043.5:c.351G>A
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ENSP00000397593.2:p.Leu117=
|
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ENST00000579462.1:n.376G>A
|
|
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ENST00000580318.1:n.540G>A
|
|
|
ENST00000582627.1:c.351G>A
|
ENSP00000462280.1:p.Leu117=
|
|
ENST00000582678.5:c.351G>A
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ENSP00000462995.1:p.Leu117=
|
|
ENST00000583336.5:n.385G>A
|
|
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ENST00000584529.5:n.385G>A
|
|
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NM_000789.3:c.351G>A
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NP_000780.1:p.Leu117=
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XM_005257110.1:c.-105G>A
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XP_005257167.1:n.-105G>A
|
|
NM_000789.4:c.351G>A
MANE Select
|
NP_000780.1:p.Leu117=
|
|
NM_001382700.1:c.116G>A
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NP_001369629.1:p.Cys39Tyr
|
|
NM_001382701.1:c.-264G>A
|
NP_001369630.1:n.-264G>A
|
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