ENST00000697124.1:n.1237C>G
|
|
|
ENST00000219596.6:c.2116C>G
MANE Select
|
ENSP00000219596.1:p.Pro706Ala
|
|
ENST00000219596.5:c.2116C>G
|
ENSP00000219596.1:p.Pro706Ala
|
|
ENST00000339854.8:c.1576C>G
|
ENSP00000339639.4:p.Pro526Ala
|
|
ENST00000536379.5:c.1483C>G
|
ENSP00000445079.1:p.Pro495Ala
|
|
ENST00000536980.5:c.*392C>G
|
ENSP00000444178.1:n.*392C>G
|
|
ENST00000537682.5:c.*392C>G
|
ENSP00000438611.1:n.*392C>G
|
|
ENST00000538326.5:c.*741C>G
|
ENSP00000437486.1:n.*741C>G
|
|
ENST00000539145.5:c.1037C>G
|
ENSP00000444471.1:n.1037C>G
|
|
ENST00000541159.5:c.1658C>G
|
ENSP00000438711.1:n.1658C>G
|
|
ENST00000542898.5:c.*392C>G
|
ENSP00000444615.1:n.*392C>G
|
|
ENST00000570511.5:c.1521C>G
|
ENSP00000458312.1:n.1521C>G
|
|
ENST00000572244.5:c.806C>G
|
ENSP00000461186.1:n.806C>G
|
|
ENST00000574583.5:c.888C>G
|
ENSP00000460269.1:n.888C>G
|
|
ENST00000576315.5:c.921C>G
|
ENSP00000460551.1:n.921C>G
|
|
ENST00000621655.1:c.1653C>G
|
ENSP00000481436.1:n.1653C>G
|
|
NM_000243.2:c.2116C>G , LRG_190t1:c.2116C>G
|
NP_000234.1:p.Pro706Ala
|
|
NM_001198536.1:c.*320C>G
|
NP_001185465.1:n.*320C>G
|
|
XM_017023236.2:c.2113C>G
|
XP_016878725.1:p.Pro705Ala
|
|
NM_000243.3:c.2116C>G
MANE Select
|
NP_000234.1:p.Pro706Ala
|
|
NM_001198536.2:c.*320C>G
|
NP_001185465.2:n.*320C>G
|
|