ENST00000697291.1:c.*2398A>C
|
ENSP00000513228.1:n.*2398A>C
|
|
ENST00000648433.1:c.2684A>C
|
ENSP00000496816.1:p.Glu895Ala
|
|
ENST00000649426.1:n.45A>C
|
|
|
ENST00000649554.1:n.2411A>C
|
|
|
ENST00000649979.2:c.2801A>C
MANE Select
|
ENSP00000497271.1:p.Glu934Ala
|
|
ENST00000679938.1:c.2489A>C
|
ENSP00000505518.1:p.Glu830Ala
|
|
ENST00000263642.2:c.2801A>C
|
ENSP00000263642.2:p.Glu934Ala
|
|
NM_022168.3:c.2801A>C
|
NP_071451.2:p.Glu934Ala
|
|
XM_011511628.1:c.2084A>C
|
XP_011509930.1:p.Glu695Ala
|
|
NM_022168.4:c.2801A>C
MANE Select
|
NP_071451.2:p.Glu934Ala
|
|