ENST00000697291.1:c.*2483C>G
|
ENSP00000513228.1:n.*2483C>G
|
|
ENST00000648433.1:c.2769C>G
|
ENSP00000496816.1:p.Cys923Trp
|
|
ENST00000649426.1:n.647C>G
|
|
|
ENST00000649554.1:n.2496C>G
|
|
|
ENST00000649979.2:c.2886C>G
MANE Select
|
ENSP00000497271.1:p.Cys962Trp
|
|
ENST00000679938.1:c.2574C>G
|
ENSP00000505518.1:p.Cys858Trp
|
|
ENST00000263642.2:c.2886C>G
|
ENSP00000263642.2:p.Cys962Trp
|
|
NM_022168.3:c.2886C>G
|
NP_071451.2:p.Cys962Trp
|
|
XM_011511628.1:c.2169C>G
|
XP_011509930.1:p.Cys723Trp
|
|
NM_022168.4:c.2886C>G
MANE Select
|
NP_071451.2:p.Cys962Trp
|
|