|
NM_001303256.3:c.2776A>G
MANE Select
|
NP_001290185.1:p.Ser926Gly
|
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ENST00000397641.8:c.2776A>G
MANE Select
|
ENSP00000380763.2:p.Ser926Gly
|
|
NM_001303256.1:c.2776A>G
|
NP_001290185.1:p.Ser926Gly
|
|
NM_001303256.2:c.2776A>G
|
NP_001290185.1:p.Ser926Gly
|
|
NM_001303257.1:c.2776A>G
|
NP_001290186.1:p.Ser926Gly
|
|
NM_001303257.2:c.2776A>G
|
NP_001290186.1:p.Ser926Gly
|
|
NM_014941.2:c.2590A>G
|
NP_055756.1:p.Ser864Gly
|
|
NM_014941.3:c.2590A>G
|
NP_055756.1:p.Ser864Gly
|
|
ENST00000215862.8:c.2590A>G
|
ENSP00000215862.4:p.Ser864Gly
|
|
ENST00000397641.7:c.2776A>G
|
ENSP00000380763.2:p.Ser926Gly
|
|
ENST00000445980.5:c.260A>G
|
|
|
ENST00000674576.1:n.4222A>G
|
|
|
ENST00000674585.1:n.461A>G
|
|
|
ENST00000675027.1:n.166A>G
|
|
|
ENST00000675317.1:n.1197A>G
|
|
|
ENST00000675402.1:n.408A>G
|
|
|
ENST00000675570.1:c.632A>G
|
|
|
ENST00000675601.1:n.2618A>G
|
|
|
ENST00000675779.1:c.124A>G
|
ENSP00000502216.1:p.Ser42Gly
|
|
ENST00000675798.1:n.528A>G
|
|
|
ENST00000676215.1:n.3619A>G
|
|
|
ENST00000676263.1:n.1021A>G
|
|
|
XM_011530003.1:c.2800A>G
|
XP_011528305.1:p.Ser934Gly
|
|
XM_011530004.1:c.2791A>G
|
XP_011528306.1:p.Ser931Gly
|
|
XM_011530004.2:c.2791A>G
|
XP_011528306.1:p.Ser931Gly
|
|
XM_011530005.1:c.2800A>G
|
XP_011528307.1:p.Ser934Gly
|
|
XM_011530006.1:c.2641A>G
|
XP_011528308.1:p.Ser881Gly
|
|
XM_017028667.2:c.2791A>G
|
XP_016884156.1:p.Ser931Gly
|