ENST00000370086.8:c.367G>T
MANE Select
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ENSP00000359103.3:p.Glu123Ter
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ENST00000320857.7:c.367G>T
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ENSP00000317331.3:p.Glu123Ter
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|
ENST00000370085.3:c.292G>T
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ENSP00000359102.3:p.Glu98Ter
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ENST00000370086.7:c.367G>T
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ENSP00000359103.3:p.Glu123Ter
|
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ENST00000370087.5:c.367G>T
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ENSP00000359104.1:p.Glu123Ter
|
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ENST00000447375.1:n.207G>T
|
|
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ENST00000460616.5:n.2075G>T
|
|
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ENST00000471880.5:n.570G>T
|
|
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ENST00000482902.5:n.2194G>T
|
|
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ENST00000485612.5:n.482G>T
|
|
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ENST00000486204.5:n.439G>T
|
|
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NM_001204526.1:c.400G>T
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NP_001191455.1:p.Glu134Ter
|
|
NM_001204527.1:c.391G>T
|
NP_001191456.1:p.Glu131Ter
|
|
NM_006280.2:c.367G>T
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NP_006271.1:p.Glu123Ter
|
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NR_037927.1:n.712G>T
|
|
|
XM_011531186.1:c.367G>T
|
XP_011529488.1:p.Glu123Ter
|
|
XM_011531187.1:c.367G>T
|
XP_011529489.1:p.Glu123Ter
|
|
XM_017029756.1:c.178G>T
|
XP_016885245.1:p.Glu60Ter
|
|
XM_017029757.1:c.178G>T
|
XP_016885246.1:p.Glu60Ter
|
|
XM_024452428.1:c.178G>T
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XP_024308196.1:p.Glu60Ter
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NM_001204527.2:c.391G>T
|
NP_001191456.1:p.Glu131Ter
|
|
NM_006280.3:c.367G>T
MANE Select
|
NP_006271.1:p.Glu123Ter
|
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