|
ENST00000348127.11:c.303C>G
|
ENSP00000265385.8:p.Thr101=
|
|
|
ENST00000484496.6:n.267C>G
|
|
|
|
ENST00000338791.11:c.411C>G
MANE Select
|
ENSP00000345096.6:p.Thr137=
|
|
|
ENST00000648462.1:c.58C>G
|
|
|
|
ENST00000338791.10:c.411C>G
|
ENSP00000345096.6:p.Thr137=
|
|
|
ENST00000348127.10:c.303C>G
|
ENSP00000265385.8:p.Thr101=
|
|
|
ENST00000354269.9:c.381C>G
|
ENSP00000346219.5:p.Thr127=
|
|
|
ENST00000419067.6:c.312C>G
|
ENSP00000399400.2:p.Thr104=
|
|
|
ENST00000469328.5:c.157C>G
|
|
|
|
ENST00000470772.5:c.156C>G
|
ENSP00000417296.1:p.Thr52=
|
|
|
ENST00000473463.1:c.*157C>G
|
ENSP00000420469.1:n.*157C>G
|
|
|
ENST00000480861.5:c.156C>G
|
ENSP00000420185.1:p.Thr52=
|
|
|
ENST00000484496.5:c.267C>G
|
ENSP00000418742.1:p.Thr89=
|
|
|
ENST00000489263.1:c.204C>G
|
ENSP00000418592.1:p.Thr68=
|
|
|
ENST00000491376.5:n.580C>G
|
|
|
|
ENST00000496200.5:c.156C>G
|
ENSP00000420803.1:p.Thr52=
|
|
|
ENST00000496487.5:n.231C>G
|
|
|
|
ENST00000497868.5:c.204C>G
|
ENSP00000419609.1:p.Thr68=
|
|
|
ENST00000626419.2:c.156C>G
|
ENSP00000486056.1:p.Thr52=
|
|
|
NM_000883.3:c.411C>G
|
NP_000874.2:p.Thr137=
|
|
|
NM_001102605.1:c.381C>G
|
NP_001096075.1:p.Thr127=
|
|
|
NM_001142573.1:c.156C>G
|
NP_001136045.1:p.Thr52=
|
|
|
NM_001142574.1:c.156C>G
|
NP_001136046.1:p.Thr52=
|
|
|
NM_001142575.1:c.156C>G
|
NP_001136047.1:p.Thr52=
|
|
|
NM_001142576.1:c.312C>G
|
NP_001136048.1:p.Thr104=
|
|
|
NM_001304521.1:c.204C>G
|
NP_001291450.1:p.Thr68=
|
|
|
NM_183243.2:c.303C>G
|
NP_899066.1:p.Thr101=
|
|
|
XM_005250314.1:c.180C>G
|
XP_005250371.1:p.Thr60=
|
|
|
XM_006715967.1:c.411C>G
|
XP_006716030.1:p.Thr137=
|
|
|
XM_006715968.1:c.381C>G
|
XP_006716031.1:p.Thr127=
|
|
|
XM_006715969.1:c.303C>G
|
XP_006716032.1:p.Thr101=
|
|
|
XM_006715970.2:c.204C>G
|
XP_006716033.1:p.Thr68=
|
|
|
XM_006715971.1:c.180C>G
|
XP_006716034.1:p.Thr60=
|
|
|
XM_017012172.1:c.180C>G
|
XP_016867661.1:p.Thr60=
|
|
|
XM_017012173.1:c.381C>G
|
XP_016867662.1:p.Thr127=
|
|
|
XM_024446755.1:c.381C>G
|
XP_024302523.1:p.Thr127=
|
|
|
XM_024446756.1:c.303C>G
|
XP_024302524.1:p.Thr101=
|
|
|
XM_024446757.1:c.204C>G
|
XP_024302525.1:p.Thr68=
|
|
|
XM_024446758.1:c.180C>G
|
XP_024302526.1:p.Thr60=
|
|
|
NM_000883.4:c.411C>G
MANE Select
|
NP_000874.2:p.Thr137=
|
|
|
NM_001102605.2:c.381C>G
|
NP_001096075.1:p.Thr127=
|
|
|
NM_001142573.2:c.156C>G
|
NP_001136045.1:p.Thr52=
|
|
|
NM_001142574.2:c.156C>G
|
NP_001136046.1:p.Thr52=
|
|
|
NM_001142575.2:c.156C>G
|
NP_001136047.1:p.Thr52=
|
|
|
NM_001142576.2:c.312C>G
|
NP_001136048.1:p.Thr104=
|
|
|
NM_001304521.2:c.204C>G
|
NP_001291450.1:p.Thr68=
|
|
|
NM_183243.3:c.303C>G
|
NP_899066.1:p.Thr101=
|
|
