ENST00000547103.7:c.6166G>T
MANE Select
|
ENSP00000447211.2:p.Glu2056Ter
|
|
ENST00000642294.1:c.106G>T
|
ENSP00000493572.1:p.Glu36Ter
|
|
ENST00000646859.1:c.6031G>T
|
ENSP00000496036.1:p.Glu2011Ter
|
|
ENST00000298820.7:c.1467G>T
|
|
|
ENST00000458043.6:c.6139G>T
|
ENSP00000400895.2:p.Glu2047Ter
|
|
ENST00000546620.5:n.422G>T
|
|
|
ENST00000547103.5:c.6103G>T
|
ENSP00000447211.1:p.Glu2035Ter
|
|
ENST00000550182.2:c.190G>T
|
ENSP00000449641.1:p.Glu64Ter
|
|
ENST00000551340.5:c.294G>T
|
|
|
NM_173591.3:c.6139G>T
|
NP_775862.3:p.Glu2047Ter
|
|
XM_005268802.2:c.6190G>T
|
XP_005268859.1:p.Glu2064Ter
|
|
XM_011538191.1:c.6190G>T
|
XP_011536493.1:p.Glu2064Ter
|
|
XM_011538192.1:c.6037G>T
|
XP_011536494.1:p.Glu2013Ter
|
|
XM_011538193.1:c.5824G>T
|
XP_011536495.1:p.Glu1942Ter
|
|
XM_005268802.3:c.6190G>T
|
XP_005268859.1:p.Glu2064Ter
|
|
XM_011538192.2:c.6037G>T
|
XP_011536494.1:p.Glu2013Ter
|
|
NM_001368062.1:c.6004G>T
|
NP_001354991.1:p.Glu2002Ter
|
|
NM_001368062.3:c.6031G>T
|
NP_001354991.2:p.Glu2011Ter
|
|
NM_001378609.3:c.6166G>T
MANE Select
|
NP_001365538.2:p.Glu2056Ter
|
|
NM_001378610.3:c.6166G>T
|
NP_001365539.2:p.Glu2056Ter
|
|
NM_173591.7:c.6166G>T
|
NP_775862.4:p.Glu2056Ter
|
|