ENST00000347401.8:c.1261G>T
|
|
|
ENST00000353578.9:c.7998G>T
|
ENSP00000315873.4:p.Thr2666=
|
|
ENST00000682957.1:c.743G>T
|
|
|
ENST00000684508.1:n.883G>T
|
|
|
ENST00000295550.9:c.8616G>T
MANE Select
|
ENSP00000295550.4:p.Thr2872=
|
|
ENST00000295550.8:c.8616G>T
|
ENSP00000295550.4:p.Thr2872=
|
|
ENST00000347401.7:c.6792G>T
|
ENSP00000315609.4:p.Thr2264=
|
|
ENST00000353578.8:c.7998G>T
|
ENSP00000315873.4:p.Thr2666=
|
|
ENST00000409809.5:c.7998G>T
|
ENSP00000386844.1:p.Thr2666=
|
|
ENST00000472056.5:c.6795G>T
|
ENSP00000418285.1:p.Thr2265=
|
|
ENST00000491769.1:n.5058G>T
|
|
|
NM_004369.3:c.8616G>T , LRG_473t1:c.8616G>T
|
NP_004360.2:p.Thr2872=
|
|
NM_057166.4:c.6795G>T
|
NP_476507.3:p.Thr2265=
|
|
NM_057167.3:c.7998G>T
|
NP_476508.2:p.Thr2666=
|
|
XM_005246065.1:c.8016G>T
|
XP_005246122.1:p.Thr2672=
|
|
XM_005246066.1:c.7395G>T
|
XP_005246123.1:p.Thr2465=
|
|
XM_006712253.1:c.8115G>T
|
XP_006712316.1:p.Thr2705=
|
|
XM_011510574.1:c.8613G>T
|
XP_011508876.1:p.Thr2871=
|
|
XM_011510575.1:c.6210G>T
|
XP_011508877.1:p.Thr2070=
|
|
XM_017003304.1:c.6210G>T
|
XP_016858793.1:p.Thr2070=
|
|
XM_024452684.1:c.7395G>T
|
XP_024308452.1:p.Thr2465=
|
|
NM_004369.4:c.8616G>T
MANE Select
|
NP_004360.2:p.Thr2872=
|
|
NM_057166.5:c.6795G>T
|
NP_476507.3:p.Thr2265=
|
|
NM_057167.4:c.7998G>T
|
NP_476508.2:p.Thr2666=
|
|