ENST00000290866.10:c.2388A>T
MANE Select
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ENSP00000290866.4:p.Arg796Ser
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ENST00000290863.10:c.666A>T
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ENSP00000290863.6:p.Arg222Ser
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ENST00000290866.9:c.2388A>T
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ENSP00000290866.4:p.Arg796Ser
|
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ENST00000413513.7:c.666A>T
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ENSP00000392247.3:p.Arg222Ser
|
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ENST00000428043.5:c.2388A>T
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ENSP00000397593.2:p.Arg796Ser
|
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ENST00000577647.2:c.666A>T
|
ENSP00000464149.1:p.Arg222Ser
|
|
ENST00000578839.5:c.*458A>T
|
ENSP00000462110.2:n.*458A>T
|
|
ENST00000579204.1:c.647A>T
|
ENSP00000464629.1:n.647A>T
|
|
ENST00000579314.5:c.*117A>T
|
ENSP00000462599.1:n.*117A>T
|
|
ENST00000582005.5:c.*308A>T
|
ENSP00000462002.1:n.*308A>T
|
|
ENST00000582761.1:c.156A>T
|
ENSP00000462909.1:p.Arg52Ser
|
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ENST00000584865.5:n.334A>T
|
|
|
NM_000789.3:c.2388A>T
|
NP_000780.1:p.Arg796Ser
|
|
NM_001178057.1:c.666A>T
|
NP_001171528.1:p.Arg222Ser
|
|
NM_152830.2:c.666A>T
|
NP_690043.1:p.Arg222Ser
|
|
XM_005257110.1:c.1839A>T
|
XP_005257167.1:p.Arg613Ser
|
|
XM_006721737.2:c.726A>T
|
XP_006721800.2:p.Arg242Ser
|
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XM_006721737.3:c.726A>T
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XP_006721800.2:p.Arg242Ser
|
|
NM_000789.4:c.2388A>T
MANE Select
|
NP_000780.1:p.Arg796Ser
|
|
NM_001178057.2:c.666A>T
|
NP_001171528.1:p.Arg222Ser
|
|
NM_152830.3:c.666A>T
|
NP_690043.1:p.Arg222Ser
|
|
NM_001382700.1:c.1821A>T
|
NP_001369629.1:p.Arg607Ser
|
|
NM_001382701.1:c.1536A>T
|
NP_001369630.1:p.Arg512Ser
|
|
NM_001382702.1:c.318A>T
|
NP_001369631.1:p.Arg106Ser
|
|
NR_168483.1:n.766A>T
|
|
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