ENST00000697124.1:n.1061G>C
|
|
|
ENST00000219596.6:c.1940G>C
MANE Select
|
ENSP00000219596.1:p.Ser647Thr
|
|
ENST00000219596.5:c.1940G>C
|
ENSP00000219596.1:p.Ser647Thr
|
|
ENST00000339854.8:c.1400G>C
|
ENSP00000339639.4:p.Ser467Thr
|
|
ENST00000536379.5:c.1307G>C
|
ENSP00000445079.1:p.Ser436Thr
|
|
ENST00000536980.5:c.*216G>C
|
ENSP00000444178.1:n.*216G>C
|
|
ENST00000537682.5:c.*216G>C
|
ENSP00000438611.1:n.*216G>C
|
|
ENST00000538326.5:c.*565G>C
|
ENSP00000437486.1:n.*565G>C
|
|
ENST00000539145.5:c.861G>C
|
ENSP00000444471.1:n.861G>C
|
|
ENST00000541159.5:c.1482G>C
|
ENSP00000438711.1:n.1482G>C
|
|
ENST00000542898.5:c.*216G>C
|
ENSP00000444615.1:n.*216G>C
|
|
ENST00000570511.5:c.1345G>C
|
ENSP00000458312.1:n.1345G>C
|
|
ENST00000572244.5:c.630G>C
|
ENSP00000461186.1:n.630G>C
|
|
ENST00000574583.5:c.712G>C
|
ENSP00000460269.1:n.712G>C
|
|
ENST00000576315.5:c.745G>C
|
ENSP00000460551.1:n.745G>C
|
|
ENST00000621655.1:c.1477G>C
|
ENSP00000481436.1:n.1477G>C
|
|
NM_000243.2:c.1940G>C , LRG_190t1:c.1940G>C
|
NP_000234.1:p.Ser647Thr
|
|
NM_001198536.1:c.*144G>C
|
NP_001185465.1:n.*144G>C
|
|
XM_017023236.2:c.1937G>C
|
XP_016878725.1:p.Ser646Thr
|
|
NM_000243.3:c.1940G>C
MANE Select
|
NP_000234.1:p.Ser647Thr
|
|
NM_001198536.2:c.*144G>C
|
NP_001185465.2:n.*144G>C
|
|