ENST00000389048.8:c.3477G>T
MANE Select
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ENSP00000373700.3:p.Gln1159His
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ENST00000431873.6:c.704G>T
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ENST00000638605.1:n.354G>T
|
|
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ENST00000642122.1:c.273G>T
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ENSP00000493203.1:p.Gln91His
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ENST00000389048.7:c.3477G>T
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ENSP00000373700.3:p.Gln1159His
|
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ENST00000431873.5:c.357G>T
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ENSP00000414027.2:p.Gln119His
|
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ENST00000453137.1:c.171G>T
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ENSP00000387488.1:p.Gln57His
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ENST00000618119.4:c.2346G>T
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ENSP00000482733.1:p.Gln782His
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NM_004304.4:c.3477G>T
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NP_004295.2:p.Gln1159His
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NM_001353765.1:c.273G>T
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NP_001340694.1:p.Gln91His
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XM_024452778.1:c.630G>T
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XP_024308546.1:p.Gln210His
|
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XM_024452779.1:c.273G>T
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XP_024308547.1:p.Gln91His
|
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NM_004304.5:c.3477G>T
MANE Select
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NP_004295.2:p.Gln1159His
|
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NM_001353765.2:c.273G>T
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NP_001340694.1:p.Gln91His
|
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