ENST00000697124.1:n.1347A>G
|
|
|
ENST00000219596.6:c.2226A>G
MANE Select
|
ENSP00000219596.1:p.Thr742=
|
|
ENST00000219596.5:c.2226A>G
|
ENSP00000219596.1:p.Thr742=
|
|
ENST00000339854.8:c.1686A>G
|
ENSP00000339639.4:p.Thr562=
|
|
ENST00000536379.5:c.1593A>G
|
ENSP00000445079.1:p.Thr531=
|
|
ENST00000536980.5:c.*502A>G
|
ENSP00000444178.1:n.*502A>G
|
|
ENST00000537682.5:c.*502A>G
|
ENSP00000438611.1:n.*502A>G
|
|
ENST00000538326.5:c.*851A>G
|
ENSP00000437486.1:n.*851A>G
|
|
ENST00000539145.5:c.1147A>G
|
ENSP00000444471.1:n.1147A>G
|
|
ENST00000541159.5:c.1768A>G
|
ENSP00000438711.1:n.1768A>G
|
|
ENST00000542898.5:c.*502A>G
|
ENSP00000444615.1:n.*502A>G
|
|
ENST00000570511.5:c.1631A>G
|
ENSP00000458312.1:n.1631A>G
|
|
ENST00000572244.5:c.916A>G
|
ENSP00000461186.1:n.916A>G
|
|
ENST00000574583.5:c.998A>G
|
ENSP00000460269.1:n.998A>G
|
|
ENST00000576315.5:c.1031A>G
|
ENSP00000460551.1:n.1031A>G
|
|
ENST00000621655.1:c.1763A>G
|
ENSP00000481436.1:n.1763A>G
|
|
NM_000243.2:c.2226A>G , LRG_190t1:c.2226A>G
|
NP_000234.1:p.Thr742=
|
|
NM_001198536.1:c.*430A>G
|
NP_001185465.1:n.*430A>G
|
|
XM_017023236.2:c.2223A>G
|
XP_016878725.1:p.Thr741=
|
|
NM_000243.3:c.2226A>G
MANE Select
|
NP_000234.1:p.Thr742=
|
|
NM_001198536.2:c.*430A>G
|
NP_001185465.2:n.*430A>G
|
|