ENST00000309755.9:c.1119G>A
MANE Select
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ENSP00000312397.4:p.Gln373=
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ENST00000309755.8:c.1119G>A
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ENSP00000312397.4:p.Gln373=
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ENST00000502381.1:n.706G>A
|
|
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ENST00000504208.5:c.*335-10616G>A
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ENSP00000423585.1:n.*335-10616G>A
|
|
ENST00000505853.1:c.999G>A
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ENSP00000426173.1:p.Gln333=
|
|
ENST00000506491.5:c.873G>A
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ENSP00000424828.1:p.Gln291=
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ENST00000506873.5:n.744G>A
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|
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ENST00000508657.5:c.1023G>A
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ENSP00000422099.1:p.Gln341=
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NM_001257194.1:c.1023G>A
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NP_001244123.1:p.Gln341=
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|
NM_001257195.1:c.873G>A
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NP_001244124.1:p.Gln291=
|
|
NM_017415.2:c.1119G>A
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NP_059111.2:p.Gln373=
|
|
NM_017415.3:c.1119G>A
MANE Select
|
NP_059111.2:p.Gln373=
|
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NM_001257195.2:c.873G>A
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NP_001244124.1:p.Gln291=
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