|
ENST00000528368.3:c.446G>T
(C1QTNF5)
MANE Select
|
ENSP00000431140.1:p.Gly149Val
|
|
|
ENST00000619721.6:c.*1342G>T
(MFRP)
MANE Select
|
ENSP00000481824.1:n.*1342G>T
|
|
|
ENST00000525657.2:n.336G>T
(C1QTNF5)
|
|
|
|
ENST00000528368.2:c.446G>T
(C1QTNF5)
|
ENSP00000431140.1:p.Gly149Val
|
|
|
ENST00000530681.2:c.446G>T
(C1QTNF5)
|
ENSP00000456533.2:p.Gly149Val
|
|
|
ENST00000619721.5:c.*1342G>T
(MFRP)
|
ENSP00000481824.1:n.*1342G>T
|
|
|
NM_001278431.1:c.446G>T
(C1QTNF5)
|
NP_001265360.1:p.Gly149Val
|
|
|
NM_015645.4:c.446G>T
(C1QTNF5)
|
NP_056460.1:p.Gly149Val
|
|
|
NM_031433.3:c.*1342G>T
(MFRP)
|
NP_113621.1:n.*1342G>T
|
|
|
NM_001278431.2:c.446G>T
(C1QTNF5)
MANE Select
|
NP_001265360.1:p.Gly149Val
|
|
|
NM_031433.4:c.*1342G>T
(MFRP)
MANE Select
|
NP_113621.1:n.*1342G>T
|
|
|
NM_015645.5:c.446G>T
(C1QTNF5)
|
NP_056460.1:p.Gly149Val
|
|
