ENST00000682089.1:n.317G>T
|
|
|
ENST00000682266.1:c.547G>T
|
ENSP00000507766.1:p.Glu183Ter
|
|
ENST00000682341.1:c.955G>T
|
ENSP00000508251.1:p.Glu319Ter
|
|
ENST00000682530.1:c.*929G>T
|
ENSP00000506805.1:n.*929G>T
|
|
ENST00000683197.1:c.955G>T
|
ENSP00000507641.1:p.Glu319Ter
|
|
ENST00000683411.1:c.547G>T
|
ENSP00000508397.1:p.Glu183Ter
|
|
ENST00000683437.1:c.547G>T
|
ENSP00000508408.1:p.Glu183Ter
|
|
ENST00000683613.1:n.1991G>T
|
|
|
ENST00000683834.1:n.1197G>T
|
|
|
ENST00000684663.1:c.952G>T
|
ENSP00000508009.1:p.Glu318Ter
|
|
ENST00000324559.9:c.997G>T
MANE Select
|
ENSP00000315371.9:p.Glu333Ter
|
|
ENST00000648804.1:n.1332G>T
|
|
|
ENST00000324559.8:c.997G>T
|
ENSP00000315371.8:p.Glu333Ter
|
|
NM_001142649.1:c.994G>T
|
NP_001136121.1:p.Glu332Ter
|
|
NM_213599.2:c.997G>T , LRG_868t1:c.997G>T
|
NP_998764.1:p.Glu333Ter
|
|
XM_005252820.2:c.955G>T
|
XP_005252877.2:p.Glu319Ter
|
|
XM_005252821.2:c.952G>T
|
XP_005252878.2:p.Glu318Ter
|
|
XM_005252822.3:c.919G>T
|
XP_005252879.1:p.Glu307Ter
|
|
XM_005252823.3:c.916G>T
|
XP_005252880.1:p.Glu306Ter
|
|
XM_011519949.1:c.904G>T
|
XP_011518251.1:p.Glu302Ter
|
|
XM_005252820.3:c.955G>T
|
XP_005252877.2:p.Glu319Ter
|
|
XM_005252821.3:c.952G>T
|
XP_005252878.2:p.Glu318Ter
|
|
XM_005252822.4:c.919G>T
|
XP_005252879.1:p.Glu307Ter
|
|
XM_011519949.2:c.904G>T
|
XP_011518251.1:p.Glu302Ter
|
|
NM_001142649.2:c.994G>T
|
NP_001136121.1:p.Glu332Ter
|
|
NM_213599.3:c.997G>T
MANE Select
|
NP_998764.1:p.Glu333Ter
|
|