ENST00000542672.7:c.1499G>C
|
ENSP00000443495.1:p.Arg500Thr
|
|
ENST00000492634.7:n.1429G>C
|
|
|
ENST00000682015.1:c.1406G>C
|
ENSP00000506961.1:p.Arg469Thr
|
|
ENST00000682692.1:n.1246G>C
|
|
|
ENST00000682966.1:n.7140G>C
|
|
|
ENST00000683111.1:c.*785G>C
|
ENSP00000507913.1:n.*785G>C
|
|
ENST00000683322.1:n.2851G>C
|
|
|
ENST00000684050.1:n.4137G>C
|
|
|
ENST00000684286.1:n.3054G>C
|
|
|
ENST00000684502.1:n.1448G>C
|
|
|
ENST00000366578.6:c.1499G>C
MANE Select
|
ENSP00000355537.4:p.Arg500Thr
|
|
ENST00000492634.6:n.1429G>C
|
|
|
ENST00000542672.6:c.1499G>C
|
ENSP00000443495.1:p.Arg500Thr
|
|
ENST00000651091.1:c.1189G>C
|
ENSP00000498677.1:n.1189G>C
|
|
ENST00000651275.1:c.1391G>C
|
ENSP00000498926.1:p.Arg464Thr
|
|
ENST00000651781.1:c.579G>C
|
|
|
ENST00000651786.1:c.*871G>C
|
ENSP00000498364.1:n.*871G>C
|
|
ENST00000652096.1:c.*904G>C
|
ENSP00000498896.1:n.*904G>C
|
|
ENST00000366578.5:c.1499G>C
|
ENSP00000355537.4:p.Arg500Thr
|
|
ENST00000492101.1:n.60G>C
|
|
|
ENST00000542672.5:c.1499G>C
|
ENSP00000443495.1:p.Arg500Thr
|
|
ENST00000546208.5:c.875G>C
|
ENSP00000438384.2:p.Arg292Thr
|
|
NM_001103.3:c.1499G>C
|
NP_001094.1:p.Arg500Thr
|
|
NM_001278343.1:c.1499G>C
|
NP_001265272.1:p.Arg500Thr
|
|
NM_001278344.1:c.875G>C
|
NP_001265273.1:p.Arg292Thr
|
|
NM_001278343.2:c.1499G>C
|
NP_001265272.1:p.Arg500Thr
|
|
NM_001103.4:c.1499G>C
MANE Select
|
NP_001094.1:p.Arg500Thr
|
|
NM_001278344.2:c.875G>C
|
NP_001265273.1:p.Arg292Thr
|
|