ENST00000290866.10:c.3880G=
MANE Select
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ENSP00000290866.4:p.Gly1294=
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|
ENST00000290863.10:c.2158G=
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ENSP00000290863.6:p.Gly720=
|
|
ENST00000290866.9:c.3880G=
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ENSP00000290866.4:p.Gly1294=
|
|
ENST00000413513.7:c.2035G=
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ENSP00000392247.3:p.Gly679=
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|
ENST00000428043.5:c.*302G=
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ENSP00000397593.2:n.*302G=
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|
ENST00000577647.2:c.1969+340G=
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ENSP00000464149.1:n.1969+340G=
|
|
ENST00000578839.5:c.*1635G=
|
ENSP00000462110.2:n.*1635G=
|
|
ENST00000579314.5:c.*1609G=
|
ENSP00000462599.1:n.*1609G=
|
|
NM_000789.3:c.3880G=
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NP_000780.1:p.Gly1294=
|
|
NM_001178057.1:c.2035G=
|
NP_001171528.1:p.Gly679=
|
|
NM_152830.2:c.2158G=
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NP_690043.1:p.Gly720=
|
|
XM_005257110.1:c.3331G=
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XP_005257167.1:p.Gly1111=
|
|
XM_006721737.2:c.2218G=
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XP_006721800.2:p.Gly740=
|
|
XM_006721737.3:c.2218G=
|
XP_006721800.2:p.Gly740=
|
|
NM_000789.4:c.3880G=
MANE Select
|
NP_000780.1:p.Gly1294=
|
|
NM_001178057.2:c.2035G=
|
NP_001171528.1:p.Gly679=
|
|
NM_152830.3:c.2158G=
|
NP_690043.1:p.Gly720=
|
|
NM_001382700.1:c.3313G=
|
NP_001369629.1:p.Gly1105=
|
|
NM_001382701.1:c.3028G=
|
NP_001369630.1:p.Gly1010=
|
|
NM_001382702.1:c.1495G=
|
NP_001369631.1:p.Gly499=
|
|
NR_168483.1:n.2258G=
|
|
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