ENST00000323929.8:c.1788C>G
MANE Select
|
ENSP00000325863.4:p.Asp596Glu
|
|
ENST00000323929.7:c.1788C>G
|
ENSP00000325863.3:p.Asp596Glu
|
|
ENST00000323977.7:c.1783+1330C>G
|
ENSP00000326094.3:n.1783+1330C>G
|
|
ENST00000393241.8:c.1785C>G
|
ENSP00000376933.4:p.Asp595Glu
|
|
ENST00000407439.7:c.1797C>G
|
ENSP00000385614.3:p.Asp599Glu
|
|
ENST00000535120.1:n.84C>G
|
|
|
NM_005590.3:c.1783+1330C>G
|
NP_005581.2:n.1783+1330C>G
|
|
NM_005591.3:c.1788C>G , LRG_85t1:c.1788C>G
|
NP_005582.1:p.Asp596Glu
|
|
XM_005274008.2:c.1320C>G
|
XP_005274065.1:p.Asp440Glu
|
|
XM_006718842.2:c.1785C>G
|
XP_006718905.1:p.Asp595Glu
|
|
XM_011542837.1:c.1788C>G
|
XP_011541139.1:p.Asp596Glu
|
|
XR_947828.1:n.2084C>G
|
|
|
NM_001330347.1:c.1785C>G
|
NP_001317276.1:p.Asp595Glu
|
|
XM_005274008.3:c.1320C>G
|
XP_005274065.1:p.Asp440Glu
|
|
XM_006718842.3:c.1785C>G
|
XP_006718905.1:p.Asp595Glu
|
|
XM_011542837.2:c.1788C>G
|
XP_011541139.1:p.Asp596Glu
|
|
XM_017017772.1:c.1788C>G
|
XP_016873261.1:p.Asp596Glu
|
|
XR_947828.2:n.2084C>G
|
|
|
NM_001330347.2:c.1785C>G
|
NP_001317276.1:p.Asp595Glu
|
|
NM_005590.4:c.1783+1330C>G
|
NP_005581.2:n.1783+1330C>G
|
|
NM_005591.4:c.1788C>G
MANE Select
|
NP_005582.1:p.Asp596Glu
|
|