ENST00000642496.1:c.3900G>C
|
|
|
ENST00000644397.2:c.5041G>C
MANE Select
|
ENSP00000495195.1:p.Asp1681His
|
|
ENST00000373965.6:c.4852G>C
|
ENSP00000363076.3:p.Asp1618His
|
|
ENST00000414778.5:c.4849G>C
|
ENSP00000410304.2:p.Asp1617His
|
|
ENST00000495484.5:c.1069G>C
|
ENSP00000480780.1:p.Asp357His
|
|
ENST00000614895.4:c.4864G>C
|
ENSP00000478512.1:p.Asp1622His
|
|
ENST00000616114.4:c.4846G>C
|
ENSP00000483745.1:p.Asp1616His
|
|
ENST00000618301.4:c.1201G>C
|
ENSP00000482780.1:p.Asp401His
|
|
ENST00000621708.4:c.4867G>C
|
ENSP00000484454.1:p.Asp1623His
|
|
NM_001142771.1:c.4867G>C
|
NP_001136243.1:p.Asp1623His
|
|
NM_001142772.1:c.4852G>C
|
NP_001136244.1:p.Asp1618His
|
|
NM_001354420.1:c.4846G>C
|
NP_001341349.1:p.Asp1616His
|
|
NM_001354429.1:c.4975G>C
|
NP_001341358.1:p.Asp1659His
|
|
XR_001747192.2:n.11333G>C
|
|
|
XR_001747193.2:n.11324G>C
|
|
|
NM_001142771.2:c.4867G>C
|
NP_001136243.1:p.Asp1623His
|
|
NM_001142772.2:c.4852G>C
|
NP_001136244.1:p.Asp1618His
|
|
NM_001354420.2:c.4846G>C
|
NP_001341349.1:p.Asp1616His
|
|
NM_001354429.2:c.4975G>C
|
NP_001341358.1:p.Asp1659His
|
|
NM_001384140.1:c.5041G>C
MANE Select
|
NP_001371069.1:p.Asp1681His
|
|