ENST00000697291.1:c.*2433G>A
|
ENSP00000513228.1:n.*2433G>A
|
|
ENST00000648433.1:c.2719G>A
|
ENSP00000496816.1:p.Ala907Thr
|
|
ENST00000649426.1:n.597G>A
|
|
|
ENST00000649554.1:n.2446G>A
|
|
|
ENST00000649979.2:c.2836G>A
MANE Select
|
ENSP00000497271.1:p.Ala946Thr
|
|
ENST00000679938.1:c.2524G>A
|
ENSP00000505518.1:p.Ala842Thr
|
|
ENST00000263642.2:c.2836G>A
|
ENSP00000263642.2:p.Ala946Thr
|
|
NM_022168.3:c.2836G>A
|
NP_071451.2:p.Ala946Thr
|
|
XM_011511628.1:c.2119G>A
|
XP_011509930.1:p.Ala707Thr
|
|
NM_022168.4:c.2836G>A
MANE Select
|
NP_071451.2:p.Ala946Thr
|
|