ENST00000215882.10:c.895G>T
MANE Select
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ENSP00000215882.5:p.Glu299Ter
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ENST00000215882.9:c.895G>T
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ENSP00000215882.5:p.Glu299Ter
|
|
ENST00000451283.5:c.586G>T
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ENSP00000401480.1:p.Glu196Ter
|
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ENST00000470922.5:n.1037G>T
|
|
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NM_001256534.1:c.916G>T
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NP_001243463.1:p.Glu306Ter
|
|
NM_001287387.1:c.586G>T
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NP_001274316.1:p.Glu196Ter
|
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NM_005984.4:c.895G>T
|
NP_005975.1:p.Glu299Ter
|
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NR_046298.2:n.946G>T
|
|
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NM_005984.5:c.895G>T
MANE Select
|
NP_005975.1:p.Glu299Ter
|
|
NM_001256534.2:c.916G>T
|
NP_001243463.1:p.Glu306Ter
|
|
NM_001287387.2:c.586G>T
|
NP_001274316.1:p.Glu196Ter
|
|
NR_046298.3:n.819G>T
|
|
|