ENST00000352410.9:c.1205A>G
MANE Select
|
ENSP00000318318.6:p.Glu402Gly
|
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ENST00000323744.10:c.1022A>G
|
ENSP00000318192.6:p.Glu341Gly
|
|
ENST00000352410.8:c.1205A>G
|
ENSP00000318318.6:p.Glu402Gly
|
|
ENST00000535694.5:c.1055A>G
|
ENSP00000440447.1:p.Glu352Gly
|
|
ENST00000563786.5:c.1145A>G
|
ENSP00000455241.1:p.Glu382Gly
|
|
ENST00000566377.5:c.*132A>G
|
ENSP00000455405.1:n.*132A>G
|
|
ENST00000566556.1:n.2230A>G
|
|
|
ENST00000567177.1:c.774A>G
|
ENSP00000457013.1:n.774A>G
|
|
NM_001289155.1:c.*132A>G
|
NP_001276084.1:n.*132A>G
|
|
NM_001289156.1:c.1055A>G
|
NP_001276085.1:p.Glu352Gly
|
|
NM_001289157.1:c.1022A>G
|
NP_001276086.1:p.Glu341Gly
|
|
NM_002435.2:c.1205A>G
|
NP_002426.1:p.Glu402Gly
|
|
XM_011521592.1:c.1193A>G
|
XP_011519894.1:p.Glu398Gly
|
|
XM_011521593.1:c.1145A>G
|
XP_011519895.1:p.Glu382Gly
|
|
NM_001330372.1:c.1145A>G
|
NP_001317301.1:p.Glu382Gly
|
|
XM_017022208.1:c.*132A>G
|
XP_016877697.1:n.*132A>G
|
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XM_017022209.2:c.*132A>G
|
XP_016877698.1:n.*132A>G
|
|
NM_002435.3:c.1205A>G
MANE Select
|
NP_002426.1:p.Glu402Gly
|
|
NM_001289155.2:c.*132A>G
|
NP_001276084.1:n.*132A>G
|
|
NM_001289156.2:c.1055A>G
|
NP_001276085.1:p.Glu352Gly
|
|
NM_001289157.2:c.1022A>G
|
NP_001276086.1:p.Glu341Gly
|
|
NM_001330372.2:c.1145A>G
|
NP_001317301.1:p.Glu382Gly
|
|