ENST00000295897.9:c.1449G>T
MANE Select
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ENSP00000295897.4:p.Gln483His
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ENST00000295897.8:c.1449G>T
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ENSP00000295897.4:p.Gln483His
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ENST00000401494.7:c.1104G>T
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ENSP00000384695.3:p.Gln368His
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ENST00000415165.6:c.873G>T
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ENSP00000401820.2:p.Gln291His
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ENST00000476441.6:c.*728G>T
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ENSP00000423727.1:n.*728G>T
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ENST00000486939.1:n.103G>T
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|
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ENST00000503124.5:c.999G>T
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ENSP00000421027.1:p.Gln333His
|
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ENST00000505649.5:n.996G>T
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|
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ENST00000509063.5:c.1449G>T
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ENSP00000422784.1:p.Gln483His
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ENST00000511370.1:c.982G>T
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|
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ENST00000621085.4:c.810G>T
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ENSP00000483421.1:p.Gln270His
|
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ENST00000621628.4:c.810G>T
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ENSP00000480485.1:p.Gln270His
|
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NM_000477.5:c.1449G>T
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NP_000468.1:p.Gln483His
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NM_000477.6:c.1449G>T
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NP_000468.1:p.Gln483His
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|
NM_000477.7:c.1449G>T
MANE Select
|
NP_000468.1:p.Gln483His
|
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