ENST00000697124.1:n.1300G>A
|
|
|
ENST00000219596.6:c.2179G>A
MANE Select
|
ENSP00000219596.1:p.Gly727Arg
|
|
ENST00000219596.5:c.2179G>A
|
ENSP00000219596.1:p.Gly727Arg
|
|
ENST00000339854.8:c.1639G>A
|
ENSP00000339639.4:p.Gly547Arg
|
|
ENST00000536379.5:c.1546G>A
|
ENSP00000445079.1:p.Gly516Arg
|
|
ENST00000536980.5:c.*455G>A
|
ENSP00000444178.1:n.*455G>A
|
|
ENST00000537682.5:c.*455G>A
|
ENSP00000438611.1:n.*455G>A
|
|
ENST00000538326.5:c.*804G>A
|
ENSP00000437486.1:n.*804G>A
|
|
ENST00000539145.5:c.1100G>A
|
ENSP00000444471.1:n.1100G>A
|
|
ENST00000541159.5:c.1721G>A
|
ENSP00000438711.1:n.1721G>A
|
|
ENST00000542898.5:c.*455G>A
|
ENSP00000444615.1:n.*455G>A
|
|
ENST00000570511.5:c.1584G>A
|
ENSP00000458312.1:n.1584G>A
|
|
ENST00000572244.5:c.869G>A
|
ENSP00000461186.1:n.869G>A
|
|
ENST00000574583.5:c.951G>A
|
ENSP00000460269.1:n.951G>A
|
|
ENST00000576315.5:c.984G>A
|
ENSP00000460551.1:n.984G>A
|
|
ENST00000621655.1:c.1716G>A
|
ENSP00000481436.1:n.1716G>A
|
|
NM_000243.2:c.2179G>A , LRG_190t1:c.2179G>A
|
NP_000234.1:p.Gly727Arg
|
|
NM_001198536.1:c.*383G>A
|
NP_001185465.1:n.*383G>A
|
|
XM_017023236.2:c.2176G>A
|
XP_016878725.1:p.Gly726Arg
|
|
NM_000243.3:c.2179G>A
MANE Select
|
NP_000234.1:p.Gly727Arg
|
|
NM_001198536.2:c.*383G>A
|
NP_001185465.2:n.*383G>A
|
|