|
NM_001303256.3:c.2270A>G
MANE Select
|
NP_001290185.1:p.Glu757Gly
|
|
ENST00000397641.8:c.2270A>G
MANE Select
|
ENSP00000380763.2:p.Glu757Gly
|
|
NM_001303256.1:c.2270A>G
|
NP_001290185.1:p.Glu757Gly
|
|
NM_001303256.2:c.2270A>G
|
NP_001290185.1:p.Glu757Gly
|
|
NM_001303257.1:c.2270A>G
|
NP_001290186.1:p.Glu757Gly
|
|
NM_001303257.2:c.2270A>G
|
NP_001290186.1:p.Glu757Gly
|
|
NM_014941.2:c.2084A>G
|
NP_055756.1:p.Glu695Gly
|
|
NM_014941.3:c.2084A>G
|
NP_055756.1:p.Glu695Gly
|
|
ENST00000215862.8:c.2084A>G
|
ENSP00000215862.4:p.Glu695Gly
|
|
ENST00000397641.7:c.2270A>G
|
ENSP00000380763.2:p.Glu757Gly
|
|
ENST00000674576.1:n.3716A>G
|
|
|
ENST00000675317.1:n.691A>G
|
|
|
ENST00000675570.1:c.42A>G
|
|
|
ENST00000675601.1:n.2112A>G
|
|
|
ENST00000676215.1:n.3113A>G
|
|
|
ENST00000676263.1:n.515A>G
|
|
|
XM_011530003.1:c.2294A>G
|
XP_011528305.1:p.Glu765Gly
|
|
XM_011530004.1:c.2285A>G
|
XP_011528306.1:p.Glu762Gly
|
|
XM_011530004.2:c.2285A>G
|
XP_011528306.1:p.Glu762Gly
|
|
XM_011530005.1:c.2294A>G
|
XP_011528307.1:p.Glu765Gly
|
|
XM_011530006.1:c.2135A>G
|
XP_011528308.1:p.Glu712Gly
|
|
XM_017028667.2:c.2285A>G
|
XP_016884156.1:p.Glu762Gly
|