ENST00000362072.8:c.912G>T
MANE Select
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ENSP00000354859.3:p.Gln304His
|
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ENST00000346454.7:c.825G>T
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ENSP00000278597.5:p.Gln275His
|
|
ENST00000362072.7:c.912G>T
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ENSP00000354859.3:p.Gln304His
|
|
ENST00000538967.5:c.918G>T
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ENSP00000438215.1:p.Gln306His
|
|
ENST00000542968.5:c.912G>T
|
ENSP00000442172.1:p.Gln304His
|
|
ENST00000544518.5:c.909G>T
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ENSP00000441068.1:p.Gln303His
|
|
NM_000795.3:c.912G>T
|
NP_000786.1:p.Gln304His
|
|
NM_016574.3:c.825G>T
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NP_057658.2:p.Gln275His
|
|
XM_017017296.2:c.912G>T
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XP_016872785.1:p.Gln304His
|
|
NM_000795.4:c.912G>T
MANE Select
|
NP_000786.1:p.Gln304His
|
|
NM_016574.4:c.825G>T
|
NP_057658.2:p.Gln275His
|
|