ENST00000699927.1:n.278G>T
(MASP2)
|
|
|
ENST00000699958.1:c.1234G>T
(MASP2)
|
ENSP00000514717.1:p.Gly412Ter
|
|
ENST00000700088.1:c.1298-759G>T
(MASP2)
|
ENSP00000514787.1:n.1298-759G>T
|
|
ENST00000700089.1:c.1336G>T
(MASP2)
|
ENSP00000514788.1:n.1336G>T
|
|
ENST00000700090.1:c.1218G>T
(MASP2)
|
ENSP00000514789.1:n.1218G>T
|
|
ENST00000700091.1:c.1141G>T
(MASP2)
|
ENSP00000514790.1:p.Gly381Ter
|
|
ENST00000700092.1:c.1318G>T
(MASP2)
|
ENSP00000514791.1:p.Gly440Ter
|
|
ENST00000700093.1:c.1315G>T
(MASP2)
|
ENSP00000514792.1:p.Gly439Ter
|
|
ENST00000700094.1:c.1347G>T
(MASP2)
|
ENSP00000514793.1:n.1347G>T
|
|
ENST00000700095.1:c.1298-759G>T
(MASP2)
|
ENSP00000514794.1:n.1298-759G>T
|
|
ENST00000700096.1:c.1101-759G>T
(MASP2)
|
ENSP00000514795.1:n.1101-759G>T
|
|
ENST00000700097.1:c.1367G>T
(MASP2)
|
ENSP00000514796.1:p.Trp456Leu
|
|
ENST00000400897.8:c.1339G>T
(MASP2)
MANE Select
|
ENSP00000383690.3:p.Gly447Ter
|
|
ENST00000400897.7:c.1339G>T
(MASP2)
|
ENSP00000383690.3:p.Gly447Ter
|
|
ENST00000611136.4:c.448+2399C>A
|
|
|
ENST00000612542.1:c.206+2399C>A
|
|
|
ENST00000614757.4:c.*452+2399C>A
|
ENSP00000481867.1:n.*452+2399C>A
|
|
ENST00000620028.1:n.416+2399C>A
|
|
|
ENST00000622108.1:c.232-2080C>A
|
ENSP00000480398.1:n.232-2080C>A
|
|
NM_006610.3:c.1339G>T
(MASP2)
|
NP_006601.2:p.Gly447Ter
|
|
XM_017000863.2:c.*3011+1942C>A
(TARDBP)
|
XP_016856352.1:n.*3011+1942C>A
|
|
XM_017000864.2:c.*1895+1942C>A
(TARDBP)
|
XP_016856353.1:n.*1895+1942C>A
|
|
XM_017000865.2:c.*1781-2080C>A
(TARDBP)
|
XP_016856354.1:n.*1781-2080C>A
|
|
NM_006610.4:c.1339G>T
(MASP2)
MANE Select
|
NP_006601.2:p.Gly447Ter
|
|