ENST00000274576.9:c.1126G>T
MANE Select
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ENSP00000274576.5:p.Ala376Ser
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ENST00000274576.8:c.1126G>T
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ENSP00000274576.4:p.Ala376Ser
|
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ENST00000455880.2:c.1150G>T
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ENSP00000411593.2:p.Ala384Ser
|
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ENST00000462581.6:c.*884G>T
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ENSP00000430595.1:n.*884G>T
|
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NM_000171.3:c.1126G>T
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NP_000162.2:p.Ala376Ser
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NM_001146040.1:c.1150G>T
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NP_001139512.1:p.Ala384Ser
|
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NM_001292000.1:c.877G>T
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NP_001278929.1:p.Ala293Ser
|
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NM_000171.4:c.1126G>T
MANE Select
|
NP_000162.2:p.Ala376Ser
|
|
NM_001146040.2:c.1150G>T
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NP_001139512.1:p.Ala384Ser
|
|
NM_001292000.2:c.877G>T
|
NP_001278929.1:p.Ala293Ser
|
|