ENST00000697291.1:c.*2478A>G
|
ENSP00000513228.1:n.*2478A>G
|
|
ENST00000648433.1:c.2764A>G
|
ENSP00000496816.1:p.Ile922Val
|
|
ENST00000649426.1:n.642A>G
|
|
|
ENST00000649554.1:n.2491A>G
|
|
|
ENST00000649979.2:c.2881A>G
MANE Select
|
ENSP00000497271.1:p.Ile961Val
|
|
ENST00000679938.1:c.2569A>G
|
ENSP00000505518.1:p.Ile857Val
|
|
ENST00000263642.2:c.2881A>G
|
ENSP00000263642.2:p.Ile961Val
|
|
NM_022168.3:c.2881A>G
|
NP_071451.2:p.Ile961Val
|
|
XM_011511628.1:c.2164A>G
|
XP_011509930.1:p.Ile722Val
|
|
NM_022168.4:c.2881A>G
MANE Select
|
NP_071451.2:p.Ile961Val
|
|