ENST00000593677.2:c.1128A>T
|
|
|
ENST00000688602.1:c.2525A>T
|
|
|
ENST00000689936.1:c.2497A>T
|
|
|
ENST00000359596.8:c.14192A>T
MANE Select
|
ENSP00000352608.2:p.Asp4731Val
|
|
ENST00000355481.8:c.14177A>T
|
ENSP00000347667.3:p.Asp4726Val
|
|
ENST00000359596.7:c.14192A>T
|
ENSP00000352608.2:p.Asp4731Val
|
|
ENST00000360985.7:c.14174A>T
|
ENSP00000354254.4:p.Asp4725Val
|
|
NM_000540.2:c.14192A>T , LRG_766t1:c.14192A>T
|
NP_000531.2:p.Asp4731Val
|
|
NM_001042723.1:c.14177A>T
|
NP_001036188.1:p.Asp4726Val
|
|
XM_006723317.1:c.14174A>T
|
XP_006723380.1:p.Asp4725Val
|
|
XM_006723319.1:c.14159A>T
|
XP_006723382.1:p.Asp4720Val
|
|
XM_011527204.1:c.14189A>T
|
XP_011525506.1:p.Asp4730Val
|
|
XM_011527205.1:c.14105A>T
|
XP_011525507.1:p.Asp4702Val
|
|
XM_006723317.2:c.14174A>T
|
XP_006723380.1:p.Asp4725Val
|
|
XM_006723319.2:c.14159A>T
|
XP_006723382.1:p.Asp4720Val
|
|
XM_011527205.2:c.14105A>T
|
XP_011525507.1:p.Asp4702Val
|
|
NM_000540.3:c.14192A>T
MANE Select
|
NP_000531.2:p.Asp4731Val
|
|
NM_001042723.2:c.14177A>T
|
NP_001036188.1:p.Asp4726Val
|
|