ENST00000617924.6:c.2235C>G
(THBS2)
MANE Select
|
ENSP00000482784.1:p.Asp745Glu
|
|
ENST00000649844.1:c.2250C>G
(THBS2)
|
ENSP00000497834.1:p.Asp750Glu
|
|
ENST00000676498.1:c.2235C>G
(THBS2)
|
ENSP00000504820.1:p.Asp745Glu
|
|
ENST00000676628.1:c.2061C>G
(THBS2)
|
ENSP00000504416.1:p.Asp687Glu
|
|
ENST00000676760.1:c.2235C>G
(THBS2)
|
ENSP00000503020.1:p.Asp745Glu
|
|
ENST00000676869.1:c.2064C>G
(THBS2)
|
ENSP00000504488.1:p.Asp688Glu
|
|
ENST00000676941.1:c.1344C>G
(THBS2)
|
ENSP00000503028.1:p.Asp448Glu
|
|
ENST00000677429.1:c.*1601C>G
(THBS2)
|
ENSP00000503286.1:n.*1601C>G
|
|
ENST00000678378.1:n.1620C>G
(THBS2)
|
|
|
ENST00000366787.7:c.2235C>G
(THBS2)
|
ENSP00000355751.3:p.Asp745Glu
|
|
ENST00000617924.4:c.2235C>G
(THBS2)
|
ENSP00000482784.1:p.Asp745Glu
|
|
NM_003247.3:c.2235C>G
(THBS2)
|
NP_003238.2:p.Asp745Glu
|
|
XR_943307.1:n.682-9629G>C
(THBS2-AS1)
|
|
|
NR_134621.1:n.682-9629G>C
(THBS2-AS1)
|
|
|
NM_003247.4:c.2235C>G
(THBS2)
|
NP_003238.2:p.Asp745Glu
|
|
NM_001381939.1:c.2061C>G
(THBS2)
|
NP_001368868.1:p.Asp687Glu
|
|
NM_001381942.1:c.2004C>G
(THBS2)
|
NP_001368871.1:p.Asp668Glu
|
|
NM_003247.5:c.2235C>G
(THBS2)
MANE Select
|
NP_003238.2:p.Asp745Glu
|
|
NR_167744.1:n.2380C>G
(THBS2)
|
|
|
NR_167745.1:n.2509C>G
(THBS2)
|
|
|