ENST00000272748.9:c.361G>T
MANE Select
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ENSP00000272748.4:p.Glu121Ter
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ENST00000272748.8:c.361G>T
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ENSP00000272748.4:p.Glu121Ter
|
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ENST00000409660.5:c.-9G>T
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ENSP00000386237.1:n.-9G>T
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ENST00000544803.5:c.361G>T
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ENSP00000440905.1:p.Glu121Ter
|
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NM_001305008.1:c.559G>T
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NP_001291937.1:p.Glu187Ter
|
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NM_001305009.1:c.361G>T
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NP_001291938.1:p.Glu121Ter
|
|
NM_001305010.1:c.367G>T
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NP_001291939.1:p.Glu123Ter
|
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NM_001305011.1:c.-9G>T
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NP_001291940.1:n.-9G>T
|
|
NM_030650.2:c.361G>T
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NP_085153.1:p.Glu121Ter
|
|
NR_130941.1:n.898G>T
|
|
|
XM_005246878.2:c.361G>T
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XP_005246935.1:p.Glu121Ter
|
|
XM_005246879.3:c.136G>T
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XP_005246936.1:p.Glu46Ter
|
|
XM_005246880.3:c.7G>T
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XP_005246937.1:p.Glu3Ter
|
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XM_006712783.2:c.361G>T
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XP_006712846.1:p.Glu121Ter
|
|
XM_011511945.1:c.136G>T
|
XP_011510247.1:p.Glu46Ter
|
|
XM_005246878.4:c.361G>T
|
XP_005246935.1:p.Glu121Ter
|
|
XM_005246879.4:c.136G>T
|
XP_005246936.1:p.Glu46Ter
|
|
XM_011511945.2:c.136G>T
|
XP_011510247.1:p.Glu46Ter
|
|
XM_017005055.1:c.-9G>T
|
XP_016860544.1:n.-9G>T
|
|
NM_030650.3:c.361G>T
MANE Select
|
NP_085153.1:p.Glu121Ter
|
|
NM_001305011.2:c.-9G>T
|
NP_001291940.1:n.-9G>T
|
|
NR_130941.2:n.879G>T
|
|
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