ENST00000697124.1:n.1448G>C
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|
|
ENST00000219596.6:c.2327G>C
MANE Select
|
ENSP00000219596.1:p.Gly776Ala
|
|
ENST00000219596.5:c.2327G>C
|
ENSP00000219596.1:p.Gly776Ala
|
|
ENST00000339854.8:c.1787G>C
|
ENSP00000339639.4:p.Gly596Ala
|
|
ENST00000536379.5:c.1694G>C
|
ENSP00000445079.1:p.Gly565Ala
|
|
ENST00000536980.5:c.*603G>C
|
ENSP00000444178.1:n.*603G>C
|
|
ENST00000537682.5:c.*603G>C
|
ENSP00000438611.1:n.*603G>C
|
|
ENST00000538326.5:c.*952G>C
|
ENSP00000437486.1:n.*952G>C
|
|
ENST00000539145.5:c.1248G>C
|
ENSP00000444471.1:n.1248G>C
|
|
ENST00000541159.5:c.1869G>C
|
ENSP00000438711.1:n.1869G>C
|
|
ENST00000542898.5:c.*603G>C
|
ENSP00000444615.1:n.*603G>C
|
|
ENST00000570511.5:c.1732G>C
|
ENSP00000458312.1:n.1732G>C
|
|
ENST00000572244.5:c.1017G>C
|
ENSP00000461186.1:n.1017G>C
|
|
ENST00000574583.5:c.1099G>C
|
ENSP00000460269.1:n.1099G>C
|
|
ENST00000576315.5:c.1132G>C
|
ENSP00000460551.1:n.1132G>C
|
|
ENST00000621655.1:c.1864G>C
|
ENSP00000481436.1:n.1864G>C
|
|
NM_000243.2:c.2327G>C , LRG_190t1:c.2327G>C
|
NP_000234.1:p.Gly776Ala
|
|
NM_001198536.1:c.*531G>C
|
NP_001185465.1:n.*531G>C
|
|
XM_017023236.2:c.2324G>C
|
XP_016878725.1:p.Gly775Ala
|
|
NM_000243.3:c.2327G>C
MANE Select
|
NP_000234.1:p.Gly776Ala
|
|
NM_001198536.2:c.*531G>C
|
NP_001185465.2:n.*531G>C
|
|