ENST00000697291.1:c.*2428A>C
|
ENSP00000513228.1:n.*2428A>C
|
|
ENST00000648433.1:c.2714A>C
|
ENSP00000496816.1:p.Asn905Thr
|
|
ENST00000649426.1:n.592A>C
|
|
|
ENST00000649554.1:n.2441A>C
|
|
|
ENST00000649979.2:c.2831A>C
MANE Select
|
ENSP00000497271.1:p.Asn944Thr
|
|
ENST00000679938.1:c.2519A>C
|
ENSP00000505518.1:p.Asn840Thr
|
|
ENST00000263642.2:c.2831A>C
|
ENSP00000263642.2:p.Asn944Thr
|
|
NM_022168.3:c.2831A>C
|
NP_071451.2:p.Asn944Thr
|
|
XM_011511628.1:c.2114A>C
|
XP_011509930.1:p.Asn705Thr
|
|
NM_022168.4:c.2831A>C
MANE Select
|
NP_071451.2:p.Asn944Thr
|
|