ENST00000593677.2:c.1752A>T
|
|
|
ENST00000688602.1:c.3149A>T
|
|
|
ENST00000689936.1:c.3121A>T
|
|
|
ENST00000692547.1:n.209A>T
|
|
|
ENST00000359596.8:c.14816A>T
MANE Select
|
ENSP00000352608.2:p.Asp4939Val
|
|
ENST00000355481.8:c.14801A>T
|
ENSP00000347667.3:p.Asp4934Val
|
|
ENST00000359596.7:c.14816A>T
|
ENSP00000352608.2:p.Asp4939Val
|
|
ENST00000360985.7:c.14798A>T
|
ENSP00000354254.4:p.Asp4933Val
|
|
NM_000540.2:c.14816A>T , LRG_766t1:c.14816A>T
|
NP_000531.2:p.Asp4939Val
|
|
NM_001042723.1:c.14801A>T
|
NP_001036188.1:p.Asp4934Val
|
|
XM_006723317.1:c.14798A>T
|
XP_006723380.1:p.Asp4933Val
|
|
XM_006723319.1:c.14783A>T
|
XP_006723382.1:p.Asp4928Val
|
|
XM_011527204.1:c.14813A>T
|
XP_011525506.1:p.Asp4938Val
|
|
XM_011527205.1:c.14729A>T
|
XP_011525507.1:p.Asp4910Val
|
|
XM_006723317.2:c.14798A>T
|
XP_006723380.1:p.Asp4933Val
|
|
XM_006723319.2:c.14783A>T
|
XP_006723382.1:p.Asp4928Val
|
|
XM_011527205.2:c.14729A>T
|
XP_011525507.1:p.Asp4910Val
|
|
NM_000540.3:c.14816A>T
MANE Select
|
NP_000531.2:p.Asp4939Val
|
|
NM_001042723.2:c.14801A>T
|
NP_001036188.1:p.Asp4934Val
|
|