ENST00000299506.3:c.75G>T
MANE Select
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ENSP00000299506.3:p.Gln25His
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ENST00000299506.2:c.75G>T
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ENSP00000299506.2:p.Gln25His
|
|
ENST00000305253.8:c.240G>T
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ENSP00000305426.4:p.Gln80His
|
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ENST00000534099.5:c.93G>T
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ENSP00000434400.1:p.Gln31His
|
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NM_003320.4:c.240G>T
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NP_003311.2:p.Gln80His
|
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NM_177972.2:c.75G>T
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NP_813977.1:p.Gln25His
|
|
XM_005253109.2:c.201G>T
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XP_005253166.1:p.Gln67His
|
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XM_011520344.1:c.111G>T
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XP_011518646.1:p.Gln37His
|
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XM_005253109.3:c.201G>T
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XP_005253166.1:p.Gln67His
|
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XM_011520344.2:c.111G>T
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XP_011518646.1:p.Gln37His
|
|
NM_177972.3:c.75G>T
MANE Select
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NP_813977.1:p.Gln25His
|
|
NM_003320.5:c.240G>T
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NP_003311.2:p.Gln80His
|
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