ENST00000301071.12:c.768G>T
MANE Select
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ENSP00000301071.7:p.Gln256His
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ENST00000547939.6:c.663G>T
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ENSP00000450268.2:p.Gln221His
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ENST00000550767.6:c.663G>T
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ENSP00000446637.1:p.Gln221His
|
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ENST00000550811.2:n.1801G>T
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|
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ENST00000552924.2:c.663G>T
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ENSP00000448725.2:p.Gln221His
|
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ENST00000679733.1:c.*224G>T
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ENSP00000505459.1:n.*224G>T
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ENST00000295766.9:c.768G>T
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ENSP00000439020.2:p.Gln256His
|
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ENST00000301071.11:c.768G>T
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ENSP00000301071.7:p.Gln256His
|
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ENST00000550767.5:c.663G>T
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ENSP00000446637.1:p.Gln221His
|
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NM_001270399.1:c.768G>T
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NP_001257328.1:p.Gln256His
|
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NM_001270400.1:c.663G>T
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NP_001257329.1:p.Gln221His
|
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NM_006009.3:c.768G>T
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NP_006000.2:p.Gln256His
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NM_006009.4:c.768G>T
MANE Select
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NP_006000.2:p.Gln256His
|
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NM_001270399.2:c.768G>T
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NP_001257328.1:p.Gln256His
|
|
NM_001270400.2:c.663G>T
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NP_001257329.1:p.Gln221His
|
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