ENST00000404085.7:c.459C>G
MANE Select
|
ENSP00000384008.3:p.Gly153=
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ENST00000404261.9:c.459C>G
|
ENSP00000384753.6:p.Gly153=
|
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ENST00000594072.6:c.459C>G
|
ENSP00000468845.4:p.Gly153=
|
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ENST00000651416.1:n.676C>G
|
|
|
ENST00000652132.1:c.426C>G
|
ENSP00000498416.1:p.Gly142=
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|
ENST00000394458.7:c.621C>G
|
ENSP00000377971.4:p.Gly207=
|
|
ENST00000404085.5:c.*358C>G
|
ENSP00000384008.2:n.*358C>G
|
|
ENST00000404261.8:c.621C>G
|
ENSP00000384753.5:p.Gly207=
|
|
ENST00000594072.5:c.621C>G
|
ENSP00000468845.3:p.Gly207=
|
|
ENST00000596099.1:n.360C>G
|
|
|
ENST00000596626.1:n.572C>G
|
|
|
ENST00000596834.1:n.507C>G
|
|
|
ENST00000598347.2:c.461C>G
|
|
|
NM_001278443.1:c.588C>G
|
NP_001265372.1:p.Gly196=
|
|
NM_001278444.1:c.621C>G
|
NP_001265373.1:p.Gly207=
|
|
NM_001278445.1:c.525C>G
|
NP_001265374.1:p.Gly175=
|
|
NM_152363.5:c.621C>G
|
NP_689576.5:p.Gly207=
|
|
NR_103530.1:n.735C>G
|
|
|
NM_001278443.2:c.426C>G
|
NP_001265372.2:p.Gly142=
|
|
NM_001278444.2:c.459C>G
|
NP_001265373.2:p.Gly153=
|
|
NM_001278445.2:c.417C>G
|
NP_001265374.2:p.Gly139=
|
|
NM_152363.6:c.459C>G
MANE Select
|
NP_689576.6:p.Gly153=
|
|
NR_103530.2:n.479C>G
|
|
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