ENST00000333891.14:c.14532G>T
MANE Select
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ENSP00000334319.8:p.Gln4844His
|
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ENST00000333891.13:c.14532G>T
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ENSP00000334319.8:p.Gln4844His
|
|
ENST00000423517.6:c.14532G>T
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ENSP00000388393.2:p.Gln4844His
|
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ENST00000426442.6:n.1027G>T
|
|
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ENST00000618073.1:c.795G>T
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ENSP00000482390.1:p.Gln265His
|
|
NM_014510.2:c.14532G>T
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NP_055325.2:p.Gln4844His
|
|
NM_033026.5:c.14532G>T
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NP_149015.2:p.Gln4844His
|
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XM_017012006.2:c.7437G>T
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XP_016867495.1:p.Gln2479His
|
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XM_017012007.1:c.7410G>T
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XP_016867496.1:p.Gln2470His
|
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XR_001744643.2:n.16101G>T
|
|
|
NM_033026.6:c.14532G>T
MANE Select
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NP_149015.2:p.Gln4844His
|
|
NM_014510.3:c.14532G>T
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NP_055325.2:p.Gln4844His
|
|