ENST00000347401.8:c.1054G>A
|
|
|
ENST00000353578.9:c.7791G>A
|
ENSP00000315873.4:p.Glu2597=
|
|
ENST00000682957.1:c.412G>A
|
|
|
ENST00000684508.1:n.676G>A
|
|
|
ENST00000295550.9:c.8409G>A
MANE Select
|
ENSP00000295550.4:p.Glu2803=
|
|
ENST00000295550.8:c.8409G>A
|
ENSP00000295550.4:p.Glu2803=
|
|
ENST00000347401.7:c.6585G>A
|
ENSP00000315609.4:p.Glu2195=
|
|
ENST00000353578.8:c.7791G>A
|
ENSP00000315873.4:p.Glu2597=
|
|
ENST00000409809.5:c.7791G>A
|
ENSP00000386844.1:p.Glu2597=
|
|
ENST00000468792.1:n.96G>A
|
|
|
ENST00000472056.5:c.6588G>A
|
ENSP00000418285.1:p.Glu2196=
|
|
ENST00000491769.1:n.4851G>A
|
|
|
NM_004369.3:c.8409G>A , LRG_473t1:c.8409G>A
|
NP_004360.2:p.Glu2803=
|
|
NM_057166.4:c.6588G>A
|
NP_476507.3:p.Glu2196=
|
|
NM_057167.3:c.7791G>A
|
NP_476508.2:p.Glu2597=
|
|
XM_005246065.1:c.7809G>A
|
XP_005246122.1:p.Glu2603=
|
|
XM_005246066.1:c.7188G>A
|
XP_005246123.1:p.Glu2396=
|
|
XM_006712253.1:c.7908G>A
|
XP_006712316.1:p.Glu2636=
|
|
XM_011510574.1:c.8406G>A
|
XP_011508876.1:p.Glu2802=
|
|
XM_011510575.1:c.6003G>A
|
XP_011508877.1:p.Glu2001=
|
|
XM_017003304.1:c.6003G>A
|
XP_016858793.1:p.Glu2001=
|
|
XM_024452684.1:c.7188G>A
|
XP_024308452.1:p.Glu2396=
|
|
NM_004369.4:c.8409G>A
MANE Select
|
NP_004360.2:p.Glu2803=
|
|
NM_057166.5:c.6588G>A
|
NP_476507.3:p.Glu2196=
|
|
NM_057167.4:c.7791G>A
|
NP_476508.2:p.Glu2597=
|
|