ENST00000302804.12:c.634G>T
MANE Select
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ENSP00000302898.6:p.Glu212Ter
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ENST00000302804.11:c.634G>T
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ENSP00000302898.6:p.Glu212Ter
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|
ENST00000415300.6:c.577G>T
|
ENSP00000407162.1:p.Glu193Ter
|
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ENST00000448930.5:c.529G>T
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ENSP00000406798.2:p.Glu177Ter
|
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ENST00000594599.1:c.118G>T
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ENSP00000469894.1:p.Glu40Ter
|
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ENST00000596375.1:c.*195G>T
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ENSP00000470465.1:n.*195G>T
|
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ENST00000598785.5:c.532G>T
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ENSP00000471830.1:p.Glu178Ter
|
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ENST00000599062.5:c.625G>T
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ENSP00000469983.1:p.Glu209Ter
|
|
ENST00000601799.5:c.*933G>T
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ENSP00000468918.1:n.*933G>T
|
|
NM_001015878.1:c.634G>T
|
NP_001015878.1:p.Glu212Ter
|
|
NM_001015879.1:c.577G>T
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NP_001015879.1:p.Glu193Ter
|
|
NM_003160.2:c.532G>T
|
NP_003151.2:p.Glu178Ter
|
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XR_430209.2:n.1528G>T
|
|
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XR_430209.3:n.1571G>T
|
|
|
NM_001015878.2:c.634G>T
MANE Select
|
NP_001015878.1:p.Glu212Ter
|
|
NM_001015879.2:c.577G>T
|
NP_001015879.1:p.Glu193Ter
|
|
NM_003160.3:c.532G>T
|
NP_003151.2:p.Glu178Ter
|
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