ENST00000333891.14:c.14439A>T
MANE Select
|
ENSP00000334319.8:p.Thr4813=
|
|
ENST00000333891.13:c.14439A>T
|
ENSP00000334319.8:p.Thr4813=
|
|
ENST00000423517.6:c.14439A>T
|
ENSP00000388393.2:p.Thr4813=
|
|
ENST00000426442.6:n.934A>T
|
|
|
ENST00000618073.1:c.702A>T
|
ENSP00000482390.1:p.Thr234=
|
|
NM_014510.2:c.14439A>T
|
NP_055325.2:p.Thr4813=
|
|
NM_033026.5:c.14439A>T
|
NP_149015.2:p.Thr4813=
|
|
XM_017012006.2:c.7344A>T
|
XP_016867495.1:p.Thr2448=
|
|
XM_017012007.1:c.7317A>T
|
XP_016867496.1:p.Thr2439=
|
|
XR_001744643.2:n.16008A>T
|
|
|
NM_033026.6:c.14439A>T
MANE Select
|
NP_149015.2:p.Thr4813=
|
|
NM_014510.3:c.14439A>T
|
NP_055325.2:p.Thr4813=
|
|