ENST00000593677.2:c.1117C>G
|
|
|
ENST00000688602.1:c.2514C>G
|
|
|
ENST00000689936.1:c.2486C>G
|
|
|
ENST00000359596.8:c.14181C>G
MANE Select
|
ENSP00000352608.2:p.Asp4727Glu
|
|
ENST00000355481.8:c.14166C>G
|
ENSP00000347667.3:p.Asp4722Glu
|
|
ENST00000359596.7:c.14181C>G
|
ENSP00000352608.2:p.Asp4727Glu
|
|
ENST00000360985.7:c.14163C>G
|
ENSP00000354254.4:p.Asp4721Glu
|
|
NM_000540.2:c.14181C>G , LRG_766t1:c.14181C>G
|
NP_000531.2:p.Asp4727Glu
|
|
NM_001042723.1:c.14166C>G
|
NP_001036188.1:p.Asp4722Glu
|
|
XM_006723317.1:c.14163C>G
|
XP_006723380.1:p.Asp4721Glu
|
|
XM_006723319.1:c.14148C>G
|
XP_006723382.1:p.Asp4716Glu
|
|
XM_011527204.1:c.14178C>G
|
XP_011525506.1:p.Asp4726Glu
|
|
XM_011527205.1:c.14094C>G
|
XP_011525507.1:p.Asp4698Glu
|
|
XM_006723317.2:c.14163C>G
|
XP_006723380.1:p.Asp4721Glu
|
|
XM_006723319.2:c.14148C>G
|
XP_006723382.1:p.Asp4716Glu
|
|
XM_011527205.2:c.14094C>G
|
XP_011525507.1:p.Asp4698Glu
|
|
NM_000540.3:c.14181C>G
MANE Select
|
NP_000531.2:p.Asp4727Glu
|
|
NM_001042723.2:c.14166C>G
|
NP_001036188.1:p.Asp4722Glu
|
|