ENST00000593677.2:c.793G>C
|
|
|
ENST00000688602.1:c.2190G>C
|
|
|
ENST00000689936.1:c.2162G>C
|
|
|
ENST00000359596.8:c.13857G>C
MANE Select
|
ENSP00000352608.2:p.Glu4619Asp
|
|
ENST00000355481.8:c.13842G>C
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ENSP00000347667.3:p.Glu4614Asp
|
|
ENST00000359596.7:c.13857G>C
|
ENSP00000352608.2:p.Glu4619Asp
|
|
ENST00000360985.7:c.13839G>C
|
ENSP00000354254.4:p.Glu4613Asp
|
|
ENST00000593677.1:c.317G>C
|
|
|
NM_000540.2:c.13857G>C , LRG_766t1:c.13857G>C
|
NP_000531.2:p.Glu4619Asp
|
|
NM_001042723.1:c.13842G>C
|
NP_001036188.1:p.Glu4614Asp
|
|
XM_006723317.1:c.13839G>C
|
XP_006723380.1:p.Glu4613Asp
|
|
XM_006723319.1:c.13824G>C
|
XP_006723382.1:p.Glu4608Asp
|
|
XM_011527204.1:c.13854G>C
|
XP_011525506.1:p.Glu4618Asp
|
|
XM_011527205.1:c.13770G>C
|
XP_011525507.1:p.Glu4590Asp
|
|
XM_006723317.2:c.13839G>C
|
XP_006723380.1:p.Glu4613Asp
|
|
XM_006723319.2:c.13824G>C
|
XP_006723382.1:p.Glu4608Asp
|
|
XM_011527205.2:c.13770G>C
|
XP_011525507.1:p.Glu4590Asp
|
|
NM_000540.3:c.13857G>C
MANE Select
|
NP_000531.2:p.Glu4619Asp
|
|
NM_001042723.2:c.13842G>C
|
NP_001036188.1:p.Glu4614Asp
|
|