ENST00000699927.1:n.564T>C
(MASP2)
|
|
|
ENST00000699958.1:c.1520T>C
(MASP2)
|
ENSP00000514717.1:p.Val507Ala
|
|
ENST00000700088.1:c.1298-473T>C
(MASP2)
|
ENSP00000514787.1:n.1298-473T>C
|
|
ENST00000700089.1:c.1622T>C
(MASP2)
|
ENSP00000514788.1:n.1622T>C
|
|
ENST00000700090.1:c.1504T>C
(MASP2)
|
ENSP00000514789.1:n.1504T>C
|
|
ENST00000700091.1:c.1427T>C
(MASP2)
|
ENSP00000514790.1:p.Val476Ala
|
|
ENST00000700092.1:c.1604T>C
(MASP2)
|
ENSP00000514791.1:p.Val535Ala
|
|
ENST00000700093.1:c.1601T>C
(MASP2)
|
ENSP00000514792.1:p.Val534Ala
|
|
ENST00000700094.1:c.1633T>C
(MASP2)
|
ENSP00000514793.1:n.1633T>C
|
|
ENST00000700095.1:c.1298-473T>C
(MASP2)
|
ENSP00000514794.1:n.1298-473T>C
|
|
ENST00000700096.1:c.1101-473T>C
(MASP2)
|
ENSP00000514795.1:n.1101-473T>C
|
|
ENST00000700097.1:c.1653T>C
(MASP2)
|
ENSP00000514796.1:n.1653T>C
|
|
ENST00000400897.8:c.1625T>C
(MASP2)
MANE Select
|
ENSP00000383690.3:p.Val542Ala
|
|
ENST00000400897.7:c.1625T>C
(MASP2)
|
ENSP00000383690.3:p.Val542Ala
|
|
ENST00000611136.4:c.448+2113A>G
|
|
|
ENST00000612542.1:c.206+2113A>G
|
|
|
ENST00000614757.4:c.*452+2113A>G
|
ENSP00000481867.1:n.*452+2113A>G
|
|
ENST00000620028.1:n.416+2113A>G
|
|
|
ENST00000622108.1:c.231+2113A>G
|
ENSP00000480398.1:n.231+2113A>G
|
|
NM_006610.3:c.1625T>C
(MASP2)
|
NP_006601.2:p.Val542Ala
|
|
XM_017000863.2:c.*3011+1656A>G
(TARDBP)
|
XP_016856352.1:n.*3011+1656A>G
|
|
XM_017000864.2:c.*1895+1656A>G
(TARDBP)
|
XP_016856353.1:n.*1895+1656A>G
|
|
XM_017000865.2:c.*1780+2113A>G
(TARDBP)
|
XP_016856354.1:n.*1780+2113A>G
|
|
NM_006610.4:c.1625T>C
(MASP2)
MANE Select
|
NP_006601.2:p.Val542Ala
|
|