ENST00000229307.9:c.414G>T
MANE Select
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ENSP00000229307.4:p.Gln138His
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ENST00000229307.8:c.414G>T
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ENSP00000229307.4:p.Gln138His
|
|
ENST00000526286.1:c.414G>T
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ENSP00000435288.1:p.Gln138His
|
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ENST00000526434.2:n.558G>T
|
|
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ENST00000541267.5:c.342G>T
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ENSP00000444434.1:p.Gln114His
|
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NM_001297698.1:c.414G>T
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NP_001284627.1:p.Gln138His
|
|
NM_024865.3:c.414G>T
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NP_079141.2:p.Gln138His
|
|
XM_011520850.1:c.414G>T
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XP_011519152.1:p.Gln138His
|
|
XM_011520851.1:c.342G>T
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XP_011519153.1:p.Gln114His
|
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XM_011520852.1:c.42G>T
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XP_011519154.1:p.Gln14His
|
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NM_024865.4:c.414G>T
MANE Select
|
NP_079141.2:p.Gln138His
|
|
NM_001297698.2:c.414G>T
|
NP_001284627.1:p.Gln138His
|
|