ENST00000697291.1:c.*941C>G
|
ENSP00000513228.1:n.*941C>G
|
|
ENST00000648433.1:c.1344C>G
|
ENSP00000496816.1:p.Thr448=
|
|
ENST00000649554.1:n.954C>G
|
|
|
ENST00000649979.2:c.1344C>G
MANE Select
|
ENSP00000497271.1:p.Thr448=
|
|
ENST00000679938.1:c.1032C>G
|
ENSP00000505518.1:p.Thr344=
|
|
ENST00000263642.2:c.1344C>G
|
ENSP00000263642.2:p.Thr448=
|
|
NM_022168.3:c.1344C>G
|
NP_071451.2:p.Thr448=
|
|
XM_011511628.1:c.627C>G
|
XP_011509930.1:p.Thr209=
|
|
XM_011511629.1:c.1344C>G
|
XP_011509931.1:p.Thr448=
|
|
NM_022168.4:c.1344C>G
MANE Select
|
NP_071451.2:p.Thr448=
|
|