ENST00000397195.10:c.998C>G
MANE Select
|
ENSP00000380378.4:p.Thr333Ser
|
|
ENST00000571495.2:n.2083C>G
|
|
|
ENST00000674608.1:c.1052C>G
|
ENSP00000501976.1:p.Thr351Ser
|
|
ENST00000674717.1:c.803C>G
|
ENSP00000501931.1:p.Thr268Ser
|
|
ENST00000675084.1:n.252C>G
|
|
|
ENST00000675202.1:c.998C>G
|
ENSP00000502843.1:p.Thr333Ser
|
|
ENST00000675331.1:c.998C>G
|
ENSP00000502031.1:p.Thr333Ser
|
|
ENST00000675385.1:n.612C>G
|
|
|
ENST00000675390.1:c.998C>G
|
ENSP00000501969.1:p.Thr333Ser
|
|
ENST00000675574.1:n.4053C>G
|
|
|
ENST00000675621.1:c.998C>G
|
ENSP00000502117.1:p.Thr333Ser
|
|
ENST00000675764.1:c.*952C>G
|
ENSP00000502242.1:n.*952C>G
|
|
ENST00000676077.1:c.*316C>G
|
ENSP00000502507.1:n.*316C>G
|
|
ENST00000676098.1:c.998C>G
|
ENSP00000502735.1:p.Thr333Ser
|
|
ENST00000676188.1:c.998C>G
|
ENSP00000502577.1:p.Thr333Ser
|
|
ENST00000676353.1:c.803C>G
|
ENSP00000502737.1:p.Thr268Ser
|
|
ENST00000397193.7:n.806C>G
|
|
|
ENST00000397195.9:c.998C>G
|
ENSP00000380378.4:p.Thr333Ser
|
|
ENST00000571495.1:n.722C>G
|
|
|
ENST00000572915.6:n.676+2506C>G
|
|
|
ENST00000574468.1:c.396+2314C>G
|
ENSP00000460591.1:n.396+2314C>G
|
|
ENST00000574816.5:n.319C>G
|
|
|
NM_000430.3:c.998C>G
|
NP_000421.1:p.Thr333Ser
|
|
XM_011523901.1:c.1052C>G
|
XP_011522203.1:p.Thr351Ser
|
|
XM_011523902.1:c.1052C>G
|
XP_011522204.1:p.Thr351Ser
|
|
XM_011523903.1:c.1052C>G
|
XP_011522205.1:p.Thr351Ser
|
|
XM_011523901.2:c.1052C>G
|
XP_011522203.1:p.Thr351Ser
|
|
XM_011523902.3:c.1052C>G
|
XP_011522204.1:p.Thr351Ser
|
|
XM_011523903.2:c.1052C>G
|
XP_011522205.1:p.Thr351Ser
|
|
XM_017024701.1:c.998C>G
|
XP_016880190.1:p.Thr333Ser
|
|
XM_017024702.2:c.803C>G
|
XP_016880191.1:p.Thr268Ser
|
|
NM_000430.4:c.998C>G
MANE Select
|
NP_000421.1:p.Thr333Ser
|
|