ENST00000358807.8:c.2909G>A
MANE Select
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ENSP00000351664.3:p.Trp970Ter
|
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ENST00000358577.7:c.2651G>A
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ENSP00000351385.3:p.Trp884Ter
|
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ENST00000358807.7:c.2909G>A
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ENSP00000351664.3:p.Trp970Ter
|
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ENST00000456101.6:n.3688G>A
|
|
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ENST00000465904.1:n.3960G>A
|
|
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ENST00000630715.2:c.2966G>A
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ENSP00000486901.1:p.Trp989Ter
|
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NM_001159291.1:c.2651G>A
|
NP_001152763.1:p.Trp884Ter
|
|
NM_001286613.1:c.2966G>A
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NP_001273542.1:p.Trp989Ter
|
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NM_022765.3:c.2909G>A
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NP_073602.3:p.Trp970Ter
|
|
NM_022765.4:c.2909G>A
MANE Select
|
NP_073602.3:p.Trp970Ter
|
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NM_001159291.2:c.2651G>A
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NP_001152763.1:p.Trp884Ter
|
|
NM_001286613.2:c.2966G>A
|
NP_001273542.1:p.Trp989Ter
|
|