ENST00000699927.1:n.447A>C
(MASP2)
|
|
|
ENST00000699958.1:c.1403A>C
(MASP2)
|
ENSP00000514717.1:p.Lys468Thr
|
|
ENST00000700088.1:c.1298-590A>C
(MASP2)
|
ENSP00000514787.1:n.1298-590A>C
|
|
ENST00000700089.1:c.1505A>C
(MASP2)
|
ENSP00000514788.1:n.1505A>C
|
|
ENST00000700090.1:c.1387A>C
(MASP2)
|
ENSP00000514789.1:n.1387A>C
|
|
ENST00000700091.1:c.1310A>C
(MASP2)
|
ENSP00000514790.1:p.Lys437Thr
|
|
ENST00000700092.1:c.1487A>C
(MASP2)
|
ENSP00000514791.1:p.Lys496Thr
|
|
ENST00000700093.1:c.1484A>C
(MASP2)
|
ENSP00000514792.1:p.Lys495Thr
|
|
ENST00000700094.1:c.1516A>C
(MASP2)
|
ENSP00000514793.1:n.1516A>C
|
|
ENST00000700095.1:c.1298-590A>C
(MASP2)
|
ENSP00000514794.1:n.1298-590A>C
|
|
ENST00000700096.1:c.1101-590A>C
(MASP2)
|
ENSP00000514795.1:n.1101-590A>C
|
|
ENST00000700097.1:c.1536A>C
(MASP2)
|
ENSP00000514796.1:n.1536A>C
|
|
ENST00000400897.8:c.1508A>C
(MASP2)
MANE Select
|
ENSP00000383690.3:p.Lys503Thr
|
|
ENST00000400897.7:c.1508A>C
(MASP2)
|
ENSP00000383690.3:p.Lys503Thr
|
|
ENST00000611136.4:c.448+2230T>G
|
|
|
ENST00000612542.1:c.206+2230T>G
|
|
|
ENST00000614757.4:c.*452+2230T>G
|
ENSP00000481867.1:n.*452+2230T>G
|
|
ENST00000620028.1:n.416+2230T>G
|
|
|
ENST00000622108.1:c.231+2230T>G
|
ENSP00000480398.1:n.231+2230T>G
|
|
NM_006610.3:c.1508A>C
(MASP2)
|
NP_006601.2:p.Lys503Thr
|
|
XM_017000863.2:c.*3011+1773T>G
(TARDBP)
|
XP_016856352.1:n.*3011+1773T>G
|
|
XM_017000864.2:c.*1895+1773T>G
(TARDBP)
|
XP_016856353.1:n.*1895+1773T>G
|
|
XM_017000865.2:c.*1780+2230T>G
(TARDBP)
|
XP_016856354.1:n.*1780+2230T>G
|
|
NM_006610.4:c.1508A>C
(MASP2)
MANE Select
|
NP_006601.2:p.Lys503Thr
|
|