ENST00000642496.1:c.3993G>T
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|
|
ENST00000644397.2:c.5134G>T
MANE Select
|
ENSP00000495195.1:p.Glu1712Ter
|
|
ENST00000373965.6:c.4945G>T
|
ENSP00000363076.3:p.Glu1649Ter
|
|
ENST00000414778.5:c.4942G>T
|
ENSP00000410304.2:p.Glu1648Ter
|
|
ENST00000495484.5:c.1162G>T
|
ENSP00000480780.1:p.Glu388Ter
|
|
ENST00000614895.4:c.4957G>T
|
ENSP00000478512.1:p.Glu1653Ter
|
|
ENST00000616114.4:c.4939G>T
|
ENSP00000483745.1:p.Glu1647Ter
|
|
ENST00000618301.4:c.1294G>T
|
ENSP00000482780.1:p.Glu432Ter
|
|
ENST00000621708.4:c.4960G>T
|
ENSP00000484454.1:p.Glu1654Ter
|
|
NM_001142771.1:c.4960G>T
|
NP_001136243.1:p.Glu1654Ter
|
|
NM_001142772.1:c.4945G>T
|
NP_001136244.1:p.Glu1649Ter
|
|
NM_001354420.1:c.4939G>T
|
NP_001341349.1:p.Glu1647Ter
|
|
NM_001354429.1:c.5068G>T
|
NP_001341358.1:p.Glu1690Ter
|
|
XR_001747192.2:n.11426G>T
|
|
|
XR_001747193.2:n.11417G>T
|
|
|
NM_001142771.2:c.4960G>T
|
NP_001136243.1:p.Glu1654Ter
|
|
NM_001142772.2:c.4945G>T
|
NP_001136244.1:p.Glu1649Ter
|
|
NM_001354420.2:c.4939G>T
|
NP_001341349.1:p.Glu1647Ter
|
|
NM_001354429.2:c.5068G>T
|
NP_001341358.1:p.Glu1690Ter
|
|
NM_001384140.1:c.5134G>T
MANE Select
|
NP_001371069.1:p.Glu1712Ter
|
|