ENST00000547103.7:c.6226G>T
MANE Select
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ENSP00000447211.2:p.Glu2076Ter
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ENST00000642294.1:c.166G>T
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ENSP00000493572.1:p.Glu56Ter
|
|
ENST00000646859.1:c.6091G>T
|
ENSP00000496036.1:p.Glu2031Ter
|
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ENST00000298820.7:c.1527G>T
|
|
|
ENST00000458043.6:c.6199G>T
|
ENSP00000400895.2:p.Glu2067Ter
|
|
ENST00000546620.5:n.482G>T
|
|
|
ENST00000547103.5:c.6163G>T
|
ENSP00000447211.1:p.Glu2055Ter
|
|
ENST00000550182.2:c.250G>T
|
ENSP00000449641.1:p.Glu84Ter
|
|
ENST00000551340.5:c.354G>T
|
|
|
NM_173591.3:c.6199G>T
|
NP_775862.3:p.Glu2067Ter
|
|
XM_005268802.2:c.6250G>T
|
XP_005268859.1:p.Glu2084Ter
|
|
XM_011538191.1:c.6250G>T
|
XP_011536493.1:p.Glu2084Ter
|
|
XM_011538192.1:c.6097G>T
|
XP_011536494.1:p.Glu2033Ter
|
|
XM_011538193.1:c.5884G>T
|
XP_011536495.1:p.Glu1962Ter
|
|
XM_005268802.3:c.6250G>T
|
XP_005268859.1:p.Glu2084Ter
|
|
XM_011538192.2:c.6097G>T
|
XP_011536494.1:p.Glu2033Ter
|
|
NM_001368062.1:c.6064G>T
|
NP_001354991.1:p.Glu2022Ter
|
|
NM_001368062.3:c.6091G>T
|
NP_001354991.2:p.Glu2031Ter
|
|
NM_001378609.3:c.6226G>T
MANE Select
|
NP_001365538.2:p.Glu2076Ter
|
|
NM_001378610.3:c.6226G>T
|
NP_001365539.2:p.Glu2076Ter
|
|
NM_173591.7:c.6226G>T
|
NP_775862.4:p.Glu2076Ter
|
|