ENST00000290866.10:c.2379G>T
MANE Select
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ENSP00000290866.4:p.Lys793Asn
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ENST00000290863.10:c.657G>T
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ENSP00000290863.6:p.Lys219Asn
|
|
ENST00000290866.9:c.2379G>T
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ENSP00000290866.4:p.Lys793Asn
|
|
ENST00000413513.7:c.657G>T
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ENSP00000392247.3:p.Lys219Asn
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ENST00000428043.5:c.2379G>T
|
ENSP00000397593.2:p.Lys793Asn
|
|
ENST00000577647.2:c.657G>T
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ENSP00000464149.1:p.Lys219Asn
|
|
ENST00000578839.5:c.*449G>T
|
ENSP00000462110.2:n.*449G>T
|
|
ENST00000579204.1:c.638G>T
|
ENSP00000464629.1:n.638G>T
|
|
ENST00000579314.5:c.*108G>T
|
ENSP00000462599.1:n.*108G>T
|
|
ENST00000582005.5:c.*299G>T
|
ENSP00000462002.1:n.*299G>T
|
|
ENST00000582761.1:c.147G>T
|
ENSP00000462909.1:p.Lys49Asn
|
|
ENST00000584865.5:n.325G>T
|
|
|
NM_000789.3:c.2379G>T
|
NP_000780.1:p.Lys793Asn
|
|
NM_001178057.1:c.657G>T
|
NP_001171528.1:p.Lys219Asn
|
|
NM_152830.2:c.657G>T
|
NP_690043.1:p.Lys219Asn
|
|
XM_005257110.1:c.1830G>T
|
XP_005257167.1:p.Lys610Asn
|
|
XM_006721737.2:c.717G>T
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XP_006721800.2:p.Lys239Asn
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|
XM_006721737.3:c.717G>T
|
XP_006721800.2:p.Lys239Asn
|
|
NM_000789.4:c.2379G>T
MANE Select
|
NP_000780.1:p.Lys793Asn
|
|
NM_001178057.2:c.657G>T
|
NP_001171528.1:p.Lys219Asn
|
|
NM_152830.3:c.657G>T
|
NP_690043.1:p.Lys219Asn
|
|
NM_001382700.1:c.1812G>T
|
NP_001369629.1:p.Lys604Asn
|
|
NM_001382701.1:c.1527G>T
|
NP_001369630.1:p.Lys509Asn
|
|
NM_001382702.1:c.309G>T
|
NP_001369631.1:p.Lys103Asn
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NR_168483.1:n.757G>T
|
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