ENST00000697124.1:n.1457G=
|
|
|
ENST00000219596.6:c.2336G=
MANE Select
|
ENSP00000219596.1:p.Gly779=
|
|
ENST00000219596.5:c.2336G=
|
ENSP00000219596.1:p.Gly779=
|
|
ENST00000339854.8:c.1796G=
|
ENSP00000339639.4:p.Gly599=
|
|
ENST00000536379.5:c.1703G=
|
ENSP00000445079.1:p.Gly568=
|
|
ENST00000536980.5:c.*612G=
|
ENSP00000444178.1:n.*612G=
|
|
ENST00000537682.5:c.*612G=
|
ENSP00000438611.1:n.*612G=
|
|
ENST00000538326.5:c.*961G=
|
ENSP00000437486.1:n.*961G=
|
|
ENST00000539145.5:c.1257G=
|
ENSP00000444471.1:n.1257G=
|
|
ENST00000541159.5:c.1878G=
|
ENSP00000438711.1:n.1878G=
|
|
ENST00000542898.5:c.*612G=
|
ENSP00000444615.1:n.*612G=
|
|
ENST00000570511.5:c.1741G=
|
ENSP00000458312.1:n.1741G=
|
|
ENST00000572244.5:c.1026G=
|
ENSP00000461186.1:n.1026G=
|
|
ENST00000574583.5:c.1108G=
|
ENSP00000460269.1:n.1108G=
|
|
ENST00000576315.5:c.1141G=
|
ENSP00000460551.1:n.1141G=
|
|
ENST00000621655.1:c.1873G=
|
ENSP00000481436.1:n.1873G=
|
|
NM_000243.2:c.2336G= , LRG_190t1:c.2336G=
|
NP_000234.1:p.Gly779=
|
|
NM_001198536.1:c.*540G=
|
NP_001185465.1:n.*540G=
|
|
XM_017023236.2:c.2333G=
|
XP_016878725.1:p.Gly778=
|
|
NM_000243.3:c.2336G=
MANE Select
|
NP_000234.1:p.Gly779=
|
|
NM_001198536.2:c.*540G=
|
NP_001185465.2:n.*540G=
|
|