ENST00000593677.2:c.1250A>G
|
|
|
ENST00000688602.1:c.2647A>G
|
|
|
ENST00000689936.1:c.2619A>G
|
|
|
ENST00000359596.8:c.14314A>G
MANE Select
|
ENSP00000352608.2:p.Ile4772Val
|
|
ENST00000355481.8:c.14299A>G
|
ENSP00000347667.3:p.Ile4767Val
|
|
ENST00000359596.7:c.14314A>G
|
ENSP00000352608.2:p.Ile4772Val
|
|
ENST00000360985.7:c.14296A>G
|
ENSP00000354254.4:p.Ile4766Val
|
|
NM_000540.2:c.14314A>G , LRG_766t1:c.14314A>G
|
NP_000531.2:p.Ile4772Val
|
|
NM_001042723.1:c.14299A>G
|
NP_001036188.1:p.Ile4767Val
|
|
XM_006723317.1:c.14296A>G
|
XP_006723380.1:p.Ile4766Val
|
|
XM_006723319.1:c.14281A>G
|
XP_006723382.1:p.Ile4761Val
|
|
XM_011527204.1:c.14311A>G
|
XP_011525506.1:p.Ile4771Val
|
|
XM_011527205.1:c.14227A>G
|
XP_011525507.1:p.Ile4743Val
|
|
XM_006723317.2:c.14296A>G
|
XP_006723380.1:p.Ile4766Val
|
|
XM_006723319.2:c.14281A>G
|
XP_006723382.1:p.Ile4761Val
|
|
XM_011527205.2:c.14227A>G
|
XP_011525507.1:p.Ile4743Val
|
|
NM_000540.3:c.14314A>G
MANE Select
|
NP_000531.2:p.Ile4772Val
|
|
NM_001042723.2:c.14299A>G
|
NP_001036188.1:p.Ile4767Val
|
|