ENST00000389048.8:c.3562C>G
MANE Select
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ENSP00000373700.3:p.Gln1188Glu
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ENST00000431873.6:c.789C>G
|
|
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ENST00000638605.1:n.439C>G
|
|
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ENST00000642122.1:c.358C>G
|
ENSP00000493203.1:p.Gln120Glu
|
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ENST00000389048.7:c.3562C>G
|
ENSP00000373700.3:p.Gln1188Glu
|
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ENST00000431873.5:c.442C>G
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ENSP00000414027.2:p.Gln148Glu
|
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ENST00000618119.4:c.2431C>G
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ENSP00000482733.1:p.Gln811Glu
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NM_004304.4:c.3562C>G
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NP_004295.2:p.Gln1188Glu
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NM_001353765.1:c.358C>G
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NP_001340694.1:p.Gln120Glu
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XM_024452778.1:c.715C>G
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XP_024308546.1:p.Gln239Glu
|
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XM_024452779.1:c.358C>G
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XP_024308547.1:p.Gln120Glu
|
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NM_004304.5:c.3562C>G
MANE Select
|
NP_004295.2:p.Gln1188Glu
|
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NM_001353765.2:c.358C>G
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NP_001340694.1:p.Gln120Glu
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