ENST00000253122.10:c.1208C>T
MANE Select
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ENSP00000253122.5:p.Ala403Val
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ENST00000253122.9:c.1208C>T
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ENSP00000253122.5:p.Ala403Val
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ENST00000413787.1:c.258-233C>T
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ENSP00000400463.1:n.258-233C>T
|
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ENST00000430077.6:c.863C>T
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ENSP00000403041.2:p.Ala288Val
|
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ENST00000442457.1:c.262C>T
|
|
|
ENST00000457723.1:c.192C>T
|
ENSP00000394742.1:p.Gly64=
|
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ENST00000467402.1:n.307C>T
|
|
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ENST00000485324.1:n.1241C>T
|
|
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NM_001142805.1:c.1178C>T
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NP_001136277.1:p.Ala393Val
|
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NM_001142806.1:c.863C>T
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NP_001136278.1:p.Ala288Val
|
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NM_005629.3:c.1208C>T
|
NP_005620.1:p.Ala403Val
|
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NM_005629.4:c.1208C>T
MANE Select
|
NP_005620.1:p.Ala403Val
|
|
NM_001142805.2:c.1178C>T
|
NP_001136277.1:p.Ala393Val
|
|