ENST00000642496.1:c.4006A>T
|
|
|
ENST00000644397.2:c.5147A>T
MANE Select
|
ENSP00000495195.1:p.Asp1716Val
|
|
ENST00000373965.6:c.4958A>T
|
ENSP00000363076.3:p.Asp1653Val
|
|
ENST00000414778.5:c.4955A>T
|
ENSP00000410304.2:p.Asp1652Val
|
|
ENST00000495484.5:c.1175A>T
|
ENSP00000480780.1:p.Asp392Val
|
|
ENST00000614895.4:c.4970A>T
|
ENSP00000478512.1:p.Asp1657Val
|
|
ENST00000616114.4:c.4952A>T
|
ENSP00000483745.1:p.Asp1651Val
|
|
ENST00000618301.4:c.1307A>T
|
ENSP00000482780.1:p.Asp436Val
|
|
ENST00000621708.4:c.4973A>T
|
ENSP00000484454.1:p.Asp1658Val
|
|
NM_001142771.1:c.4973A>T
|
NP_001136243.1:p.Asp1658Val
|
|
NM_001142772.1:c.4958A>T
|
NP_001136244.1:p.Asp1653Val
|
|
NM_001354420.1:c.4952A>T
|
NP_001341349.1:p.Asp1651Val
|
|
NM_001354429.1:c.5081A>T
|
NP_001341358.1:p.Asp1694Val
|
|
XR_001747192.2:n.11439A>T
|
|
|
XR_001747193.2:n.11430A>T
|
|
|
NM_001142771.2:c.4973A>T
|
NP_001136243.1:p.Asp1658Val
|
|
NM_001142772.2:c.4958A>T
|
NP_001136244.1:p.Asp1653Val
|
|
NM_001354420.2:c.4952A>T
|
NP_001341349.1:p.Asp1651Val
|
|
NM_001354429.2:c.5081A>T
|
NP_001341358.1:p.Asp1694Val
|
|
NM_001384140.1:c.5147A>T
MANE Select
|
NP_001371069.1:p.Asp1716Val
|
|