ENST00000233072.10:c.2349A>G
MANE Select
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ENSP00000233072.5:p.Gly783=
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ENST00000430249.7:c.2367A>G
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ENSP00000402608.2:p.Gly789=
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ENST00000451903.3:c.996A>G
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ENSP00000406136.2:p.Gly332=
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ENST00000673510.1:c.2349A>G
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ENSP00000500537.1:p.Gly783=
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ENST00000673630.1:c.2349A>G
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ENSP00000501073.1:p.Gly783=
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ENST00000673698.1:c.829A>G
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|
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ENST00000673711.1:c.2349A>G
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ENSP00000501022.1:p.Gly783=
|
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ENST00000674074.1:n.1494A>G
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|
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ENST00000233072.9:c.2349A>G
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ENSP00000233072.5:p.Gly783=
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ENST00000430249.6:c.2367A>G
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ENSP00000402608.2:p.Gly789=
|
|
ENST00000451903.2:c.996A>G
|
ENSP00000406136.2:p.Gly332=
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|
NM_001122633.2:c.2367A>G
|
NP_001116105.1:p.Gly789=
|
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NM_001122634.3:c.996A>G
|
NP_001116106.1:p.Gly332=
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NM_001875.4:c.2349A>G , LRG_336t1:c.2349A>G
|
NP_001866.2:p.Gly783=
|
|
XM_011510640.1:c.2382A>G
|
XP_011508942.1:p.Gly794=
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XM_011510641.1:c.2349A>G
|
XP_011508943.1:p.Gly783=
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XM_011510642.1:c.2349A>G
|
XP_011508944.1:p.Gly783=
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|
XM_011510643.1:c.2349A>G
|
XP_011508945.1:p.Gly783=
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|
XM_011510644.1:c.2349A>G
|
XP_011508946.1:p.Gly783=
|
|
NM_001122633.3:c.2349A>G
|
NP_001116105.2:p.Gly783=
|
|
NM_001369256.1:c.2382A>G
|
NP_001356185.1:p.Gly794=
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|
NM_001369257.1:c.2349A>G
|
NP_001356186.1:p.Gly783=
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|
NM_001875.5:c.2349A>G
MANE Select
|
NP_001866.2:p.Gly783=
|
|
NR_161225.1:n.3258A>G
|
|
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NR_163592.1:n.1505A>G
|
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