ENST00000696724.1:c.1354G>A
(IFNGR2)
|
ENSP00000512835.1:n.1354G>A
|
|
ENST00000290219.11:c.*349G>A
(IFNGR2)
MANE Select
|
ENSP00000290219.5:n.*349G>A
|
|
ENST00000290219.10:c.*349G>A
(IFNGR2)
|
ENSP00000290219.5:n.*349G>A
|
|
ENST00000381995.5:c.*349G>A
(IFNGR2)
|
ENSP00000371425.1:n.*349G>A
|
|
ENST00000405436.5:c.*349G>A
(IFNGR2)
|
ENSP00000385044.1:n.*349G>A
|
|
ENST00000420455.5:c.*2120+1903C>T
(TMEM50B)
|
ENSP00000397773.1:n.*2120+1903C>T
|
|
ENST00000421802.1:c.176+4440G>A
(IFNGR2)
|
|
|
ENST00000468874.2:n.616-319C>T
(TMEM50B)
|
|
|
ENST00000470682.5:n.359+1903C>T
(TMEM50B)
|
|
|
ENST00000484377.5:n.268-319C>T
(TMEM50B)
|
|
|
NM_005534.3:c.*349G>A , LRG_67t1:c.*349G>A
(IFNGR2)
|
NP_005525.2:n.*349G>A
|
|
NR_040016.1:n.2810+1903C>T
(TMEM50B)
|
|
|
XM_005260969.2:c.*349G>A
(IFNGR2)
|
XP_005261026.1:n.*349G>A
|
|
XM_011529553.1:c.*349G>A
(IFNGR2)
|
XP_011527855.1:n.*349G>A
|
|
XM_011529554.1:c.*349G>A
(IFNGR2)
|
XP_011527856.1:n.*349G>A
|
|
XM_011529746.1:c.*2121-319C>T
(TMEM50B)
|
XP_011528048.1:n.*2121-319C>T
|
|
NM_001329128.1:c.*349G>A
(IFNGR2)
|
NP_001316057.1:n.*349G>A
|
|
XM_011529554.2:c.*349G>A
(IFNGR2)
|
XP_011527856.1:n.*349G>A
|
|
XM_011529746.2:c.*2121-319C>T
(TMEM50B)
|
XP_011528048.1:n.*2121-319C>T
|
|
NM_001329128.2:c.*349G>A
(IFNGR2)
|
NP_001316057.1:n.*349G>A
|
|
NM_005534.4:c.*349G>A
(IFNGR2)
MANE Select
|
NP_005525.2:n.*349G>A
|
|
NR_040016.2:n.2775+1903C>T
(TMEM50B)
|
|
|