ENST00000347401.8:c.1325A=
|
|
|
ENST00000353578.9:c.8062A=
|
ENSP00000315873.4:p.Thr2688=
|
|
ENST00000682957.1:c.807A=
|
|
|
ENST00000684508.1:n.947A=
|
|
|
ENST00000295550.9:c.8680A=
MANE Select
|
ENSP00000295550.4:p.Thr2894=
|
|
ENST00000295550.8:c.8680A=
|
ENSP00000295550.4:p.Thr2894=
|
|
ENST00000347401.7:c.6856A=
|
ENSP00000315609.4:p.Thr2286=
|
|
ENST00000353578.8:c.8062A=
|
ENSP00000315873.4:p.Thr2688=
|
|
ENST00000409809.5:c.8062A=
|
ENSP00000386844.1:p.Thr2688=
|
|
ENST00000472056.5:c.6859A=
|
ENSP00000418285.1:p.Thr2287=
|
|
ENST00000491769.1:n.5122A=
|
|
|
NM_004369.3:c.8680A= , LRG_473t1:c.8680A=
|
NP_004360.2:p.Thr2894=
|
|
NM_057166.4:c.6859A=
|
NP_476507.3:p.Thr2287=
|
|
NM_057167.3:c.8062A=
|
NP_476508.2:p.Thr2688=
|
|
XM_005246065.1:c.8080A=
|
XP_005246122.1:p.Thr2694=
|
|
XM_005246066.1:c.7459A=
|
XP_005246123.1:p.Thr2487=
|
|
XM_006712253.1:c.8179A=
|
XP_006712316.1:p.Thr2727=
|
|
XM_011510574.1:c.8677A=
|
XP_011508876.1:p.Thr2893=
|
|
XM_011510575.1:c.6274A=
|
XP_011508877.1:p.Thr2092=
|
|
XM_017003304.1:c.6274A=
|
XP_016858793.1:p.Thr2092=
|
|
XM_024452684.1:c.7459A=
|
XP_024308452.1:p.Thr2487=
|
|
NM_004369.4:c.8680A=
MANE Select
|
NP_004360.2:p.Thr2894=
|
|
NM_057166.5:c.6859A=
|
NP_476507.3:p.Thr2287=
|
|
NM_057167.4:c.8062A=
|
NP_476508.2:p.Thr2688=
|
|