ENST00000642496.1:c.4029G>T
|
|
|
ENST00000644397.2:c.5170G>T
MANE Select
|
ENSP00000495195.1:p.Glu1724Ter
|
|
ENST00000373965.6:c.4981G>T
|
ENSP00000363076.3:p.Glu1661Ter
|
|
ENST00000414778.5:c.4978G>T
|
ENSP00000410304.2:p.Glu1660Ter
|
|
ENST00000495484.5:c.1198G>T
|
ENSP00000480780.1:p.Glu400Ter
|
|
ENST00000614895.4:c.4993G>T
|
ENSP00000478512.1:p.Glu1665Ter
|
|
ENST00000616114.4:c.4975G>T
|
ENSP00000483745.1:p.Glu1659Ter
|
|
ENST00000618301.4:c.1330G>T
|
ENSP00000482780.1:p.Glu444Ter
|
|
ENST00000621708.4:c.4996G>T
|
ENSP00000484454.1:p.Glu1666Ter
|
|
NM_001142771.1:c.4996G>T
|
NP_001136243.1:p.Glu1666Ter
|
|
NM_001142772.1:c.4981G>T
|
NP_001136244.1:p.Glu1661Ter
|
|
NM_001354420.1:c.4975G>T
|
NP_001341349.1:p.Glu1659Ter
|
|
NM_001354429.1:c.5104G>T
|
NP_001341358.1:p.Glu1702Ter
|
|
XR_001747192.2:n.11462G>T
|
|
|
XR_001747193.2:n.11453G>T
|
|
|
NM_001142771.2:c.4996G>T
|
NP_001136243.1:p.Glu1666Ter
|
|
NM_001142772.2:c.4981G>T
|
NP_001136244.1:p.Glu1661Ter
|
|
NM_001354420.2:c.4975G>T
|
NP_001341349.1:p.Glu1659Ter
|
|
NM_001354429.2:c.5104G>T
|
NP_001341358.1:p.Glu1702Ter
|
|
NM_001384140.1:c.5170G>T
MANE Select
|
NP_001371069.1:p.Glu1724Ter
|
|