ENST00000209873.9:c.914C>G
MANE Select
|
ENSP00000209873.4:p.Thr305Ser
|
|
ENST00000546393.7:n.1759C>G
|
|
|
ENST00000546562.6:n.1978C>G
|
|
|
ENST00000547238.6:n.1550C>G
|
|
|
ENST00000547520.6:n.908C>G
|
|
|
ENST00000547757.2:c.-38C>G
|
ENSP00000448020.2:n.-38C>G
|
|
ENST00000548880.2:n.1364C>G
|
|
|
ENST00000548931.6:c.434C>G
|
ENSP00000457518.1:p.Thr145Ser
|
|
ENST00000549450.6:n.848C>G
|
|
|
ENST00000552161.6:n.1870C>G
|
|
|
ENST00000672797.1:n.1367C>G
|
|
|
ENST00000672900.1:n.1712C>G
|
|
|
ENST00000209873.8:c.914C>G
|
ENSP00000209873.4:p.Thr305Ser
|
|
ENST00000394384.7:c.815C>G
|
ENSP00000377908.3:p.Thr272Ser
|
|
ENST00000546393.6:n.811C>G
|
|
|
ENST00000546572.1:n.366C>G
|
|
|
ENST00000547520.5:n.618C>G
|
|
|
ENST00000547757.1:c.815C>G
|
ENSP00000448020.1:p.Thr272Ser
|
|
ENST00000547761.6:n.806C>G
|
|
|
ENST00000548931.5:c.434C>G
|
ENSP00000457518.1:p.Thr145Ser
|
|
ENST00000550033.5:n.169C>G
|
|
|
ENST00000550286.5:c.542C>G
|
ENSP00000446885.1:p.Thr181Ser
|
|
ENST00000552876.5:n.1257C>G
|
|
|
NM_001173466.1:c.815C>G
|
NP_001166937.1:p.Thr272Ser
|
|
NM_015665.5:c.914C>G
|
NP_056480.1:p.Thr305Ser
|
|
XM_006719617.2:c.929C>G
|
XP_006719680.1:p.Thr310Ser
|
|
XM_006719619.2:c.929C>G
|
XP_006719682.1:p.Thr310Ser
|
|
XM_011538777.1:c.929C>G
|
XP_011537079.1:p.Thr310Ser
|
|
XM_011538778.1:c.914C>G
|
XP_011537080.1:p.Thr305Ser
|
|
XM_011538779.1:c.830C>G
|
XP_011537081.1:p.Thr277Ser
|
|
XM_011538780.1:c.815C>G
|
XP_011537082.1:p.Thr272Ser
|
|
XM_011538781.1:c.263C>G
|
XP_011537083.1:p.Thr88Ser
|
|
XM_011538778.2:c.914C>G
|
XP_011537080.1:p.Thr305Ser
|
|
XM_011538780.2:c.815C>G
|
XP_011537082.1:p.Thr272Ser
|
|
XR_001748875.2:n.935C>G
|
|
|
NM_015665.6:c.914C>G
MANE Select
|
NP_056480.1:p.Thr305Ser
|
|
NM_001173466.2:c.815C>G
|
NP_001166937.1:p.Thr272Ser
|
|