ENST00000391944.8:c.1684C>G
|
ENSP00000375808.4:p.Gln562Glu
|
|
ENST00000682414.1:c.1684C>G
|
ENSP00000507019.1:p.Gln562Glu
|
|
ENST00000682508.1:n.1713C>G
|
|
|
ENST00000684218.1:c.*942C>G
|
ENSP00000507804.1:n.*942C>G
|
|
ENST00000684264.1:n.1240C>G
|
|
|
ENST00000684407.1:c.1561C>G
|
ENSP00000507775.1:p.Gln521Glu
|
|
ENST00000684458.1:c.*170C>G
|
ENSP00000508260.1:n.*170C>G
|
|
ENST00000684468.1:n.1396C>G
|
|
|
ENST00000391945.10:c.1684C>G
MANE Select
|
ENSP00000375809.4:p.Gln562Glu
|
|
ENST00000587376.6:c.743C>G
|
|
|
ENST00000646507.1:n.1781C>G
|
|
|
ENST00000391941.6:c.1612C>G
|
ENSP00000375805.2:p.Gln538Glu
|
|
ENST00000391942.6:n.855C>G
|
|
|
ENST00000391944.7:c.1450C>G
|
ENSP00000375808.3:p.Gln484Glu
|
|
ENST00000391945.8:c.1684C>G
|
ENSP00000375809.3:p.Gln562Glu
|
|
ENST00000587376.5:c.743C>G
|
|
|
ENST00000588652.5:n.1772C>G
|
|
|
NM_000400.3:c.1684C>G , LRG_461t1:c.1684C>G
|
NP_000391.1:p.Gln562Glu
|
|
XM_011526611.1:c.1606C>G
|
XP_011524913.1:p.Gln536Glu
|
|
XR_935763.1:n.1667C>G
|
|
|
XM_011526611.2:c.1606C>G
|
XP_011524913.1:p.Gln536Glu
|
|
XM_017026467.1:c.1561C>G
|
XP_016881956.1:p.Gln521Glu
|
|
XR_001753633.2:n.1731C>G
|
|
|
XR_001753634.2:n.1667C>G
|
|
|
NM_000400.4:c.1684C>G
MANE Select
|
NP_000391.1:p.Gln562Glu
|
|