ENST00000617924.6:c.2233G>T
(THBS2)
MANE Select
|
ENSP00000482784.1:p.Asp745Tyr
|
|
ENST00000649844.1:c.2248G>T
(THBS2)
|
ENSP00000497834.1:p.Asp750Tyr
|
|
ENST00000676498.1:c.2233G>T
(THBS2)
|
ENSP00000504820.1:p.Asp745Tyr
|
|
ENST00000676628.1:c.2059G>T
(THBS2)
|
ENSP00000504416.1:p.Asp687Tyr
|
|
ENST00000676760.1:c.2233G>T
(THBS2)
|
ENSP00000503020.1:p.Asp745Tyr
|
|
ENST00000676869.1:c.2062G>T
(THBS2)
|
ENSP00000504488.1:p.Asp688Tyr
|
|
ENST00000676941.1:c.1342G>T
(THBS2)
|
ENSP00000503028.1:p.Asp448Tyr
|
|
ENST00000677429.1:c.*1599G>T
(THBS2)
|
ENSP00000503286.1:n.*1599G>T
|
|
ENST00000678378.1:n.1618G>T
(THBS2)
|
|
|
ENST00000366787.7:c.2233G>T
(THBS2)
|
ENSP00000355751.3:p.Asp745Tyr
|
|
ENST00000617924.4:c.2233G>T
(THBS2)
|
ENSP00000482784.1:p.Asp745Tyr
|
|
NM_003247.3:c.2233G>T
(THBS2)
|
NP_003238.2:p.Asp745Tyr
|
|
XR_943307.1:n.682-9627C>A
(THBS2-AS1)
|
|
|
NR_134621.1:n.682-9627C>A
(THBS2-AS1)
|
|
|
NM_003247.4:c.2233G>T
(THBS2)
|
NP_003238.2:p.Asp745Tyr
|
|
NM_001381939.1:c.2059G>T
(THBS2)
|
NP_001368868.1:p.Asp687Tyr
|
|
NM_001381942.1:c.2002G>T
(THBS2)
|
NP_001368871.1:p.Asp668Tyr
|
|
NM_003247.5:c.2233G>T
(THBS2)
MANE Select
|
NP_003238.2:p.Asp745Tyr
|
|
NR_167744.1:n.2378G>T
(THBS2)
|
|
|
NR_167745.1:n.2507G>T
(THBS2)
|
|
|