|
ENST00000444124.7:c.895T>G
(DDC)
MANE Select
|
ENSP00000403644.2:p.Phe299Val
|
|
|
ENST00000357936.9:c.895T>G
(DDC)
|
ENSP00000350616.5:p.Phe299Val
|
|
|
ENST00000380984.4:c.895T>G
(DDC)
|
ENSP00000370371.4:p.Phe299Val
|
|
|
ENST00000426377.5:c.661T>G
(DDC)
|
ENSP00000395069.1:p.Phe221Val
|
|
|
ENST00000430300.5:c.537T>G
(DDC)
|
|
|
|
ENST00000431062.5:c.616T>G
(DDC)
|
ENSP00000399184.1:p.Phe206Val
|
|
|
ENST00000444124.6:c.895T>G
(DDC)
|
ENSP00000403644.2:p.Phe299Val
|
|
|
ENST00000444733.5:c.686T>G
(DDC)
|
ENSP00000393724.1:p.Leu229Arg
|
|
|
ENST00000613602.3:c.-11+47119T>G
(FIGNL1)
|
ENSP00000481751.1:n.-11+47119T>G
|
|
|
ENST00000615193.4:c.616T>G
(DDC)
|
ENSP00000484104.1:p.Phe206Val
|
|
|
ENST00000617822.4:c.751T>G
(DDC)
|
ENSP00000478385.1:p.Phe251Val
|
|
|
ENST00000622873.4:c.781T>G
(DDC)
|
ENSP00000479110.1:p.Phe261Val
|
|
|
NM_000790.3:c.895T>G
(DDC)
|
NP_000781.1:p.Phe299Val
|
|
|
NM_001082971.1:c.895T>G
(DDC)
|
NP_001076440.1:p.Phe299Val
|
|
|
NM_001242886.1:c.781T>G
(DDC)
|
NP_001229815.1:p.Phe261Val
|
|
|
NM_001242887.1:c.751T>G
(DDC)
|
NP_001229816.1:p.Phe251Val
|
|
|
NM_001242888.1:c.661T>G
(DDC)
|
NP_001229817.1:p.Phe221Val
|
|
|
NM_001242889.1:c.616T>G
(DDC)
|
NP_001229818.1:p.Phe206Val
|
|
|
NM_001242890.1:c.895T>G
(DDC)
|
NP_001229819.1:p.Phe299Val
|
|
|
XM_005271745.3:c.781T>G
(DDC)
|
XP_005271802.1:p.Phe261Val
|
|
|
XM_011515161.1:c.544T>G
(DDC)
|
XP_011513463.1:p.Phe182Val
|
|
|
XM_005271745.4:c.781T>G
(DDC)
|
XP_005271802.1:p.Phe261Val
|
|
|
XM_011515161.2:c.838T>G
(DDC)
|
XP_011513463.2:p.Phe280Val
|
|
|
NM_001082971.2:c.895T>G
(DDC)
MANE Select
|
NP_001076440.2:p.Phe299Val
|
|
|
NM_000790.4:c.895T>G
(DDC)
|
NP_000781.2:p.Phe299Val
|
|
|
NM_001242888.2:c.661T>G
(DDC)
|
NP_001229817.2:p.Phe221Val
|
|
|
NM_001242890.2:c.895T>G
(DDC)
|
NP_001229819.2:p.Phe299Val
|
|
|
NM_001242886.2:c.781T>G
(DDC)
|
NP_001229815.2:p.Phe261Val
|
|
|
NM_001242887.2:c.751T>G
(DDC)
|
NP_001229816.2:p.Phe251Val
|
|
|
NM_001242889.2:c.616T>G
(DDC)
|
NP_001229818.2:p.Phe206Val
|
|
