ENST00000290866.10:c.3824G>T
MANE Select
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ENSP00000290866.4:p.Gly1275Val
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ENST00000290863.10:c.2102G>T
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ENSP00000290863.6:p.Gly701Val
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ENST00000290866.9:c.3824G>T
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ENSP00000290866.4:p.Gly1275Val
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ENST00000413513.7:c.1979G>T
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ENSP00000392247.3:p.Gly660Val
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ENST00000428043.5:c.*246G>T
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ENSP00000397593.2:n.*246G>T
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ENST00000577647.2:c.1969+284G>T
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ENSP00000464149.1:n.1969+284G>T
|
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ENST00000578839.5:c.*1579G>T
|
ENSP00000462110.2:n.*1579G>T
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ENST00000579314.5:c.*1553G>T
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ENSP00000462599.1:n.*1553G>T
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NM_000789.3:c.3824G>T
|
NP_000780.1:p.Gly1275Val
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NM_001178057.1:c.1979G>T
|
NP_001171528.1:p.Gly660Val
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NM_152830.2:c.2102G>T
|
NP_690043.1:p.Gly701Val
|
|
XM_005257110.1:c.3275G>T
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XP_005257167.1:p.Gly1092Val
|
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XM_006721737.2:c.2162G>T
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XP_006721800.2:p.Gly721Val
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XM_006721737.3:c.2162G>T
|
XP_006721800.2:p.Gly721Val
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|
NM_000789.4:c.3824G>T
MANE Select
|
NP_000780.1:p.Gly1275Val
|
|
NM_001178057.2:c.1979G>T
|
NP_001171528.1:p.Gly660Val
|
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NM_152830.3:c.2102G>T
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NP_690043.1:p.Gly701Val
|
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NM_001382700.1:c.3257G>T
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NP_001369629.1:p.Gly1086Val
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NM_001382701.1:c.2972G>T
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NP_001369630.1:p.Gly991Val
|
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NM_001382702.1:c.1439G>T
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NP_001369631.1:p.Gly480Val
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NR_168483.1:n.2202G>T
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