ENST00000398603.6:c.485_487delinsAGT
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ENSP00000381604.1:p.Glu162=
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ENST00000398606.10:c.593_595delinsAGT
MANE Select
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ENSP00000381607.3:p.Glu198=
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ENST00000398603.5:c.485_487delinsAGT
|
ENSP00000381604.1:p.Glu162=
|
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ENST00000398606.7:c.593_595delinsAGT
|
ENSP00000381607.3:p.Glu198=
|
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ENST00000467591.1:n.704_706delinsAGT
|
|
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ENST00000494593.1:n.1565_1567delinsAGT
|
|
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ENST00000498765.5:c.656_658delinsAGT
|
|
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NM_000852.3:c.593_595delinsAGT , LRG_723t1:c.593_595delinsAGT
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NP_000843.1:p.Glu198=
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NM_000852.4:c.593_595delinsAGT
MANE Select
|
NP_000843.1:p.Glu198=
|
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