ENST00000697291.1:c.*2495G>T
|
ENSP00000513228.1:n.*2495G>T
|
|
ENST00000648433.1:c.2781G>T
|
ENSP00000496816.1:p.Gln927His
|
|
ENST00000649426.1:n.659G>T
|
|
|
ENST00000649554.1:n.2508G>T
|
|
|
ENST00000649979.2:c.2898G>T
MANE Select
|
ENSP00000497271.1:p.Gln966His
|
|
ENST00000679938.1:c.2586G>T
|
ENSP00000505518.1:p.Gln862His
|
|
ENST00000263642.2:c.2898G>T
|
ENSP00000263642.2:p.Gln966His
|
|
NM_022168.3:c.2898G>T
|
NP_071451.2:p.Gln966His
|
|
XM_011511628.1:c.2181G>T
|
XP_011509930.1:p.Gln727His
|
|
NM_022168.4:c.2898G>T
MANE Select
|
NP_071451.2:p.Gln966His
|
|