NM_003246.4:c.1939C>T
(THBS1)
MANE Select
|
NP_003237.2:p.Arg647Cys
|
ENST00000260356.6:c.1939C>T
(THBS1)
MANE Select
|
ENSP00000260356.5:p.Arg647Cys
|
NM_003246.2:c.1939C>T
(THBS1)
|
NP_003237.2:p.Arg647Cys
|
NM_003246.3:c.1939C>T
(THBS1)
|
NP_003237.2:p.Arg647Cys
|
ENST00000260356.5:c.1939C>T
(THBS1)
|
ENSP00000260356.5:p.Arg647Cys
|
ENST00000490247.1:n.405C>T
(THBS1)
|
|
ENST00000642527.1:c.771-1243G>A
(FSIP1)
|
|
XM_011521970.1:c.1939C>T
(THBS1)
|
XP_011520272.1:p.Arg647Cys
|
XM_011521971.1:c.1765C>T
(THBS1)
|
XP_011520273.1:p.Arg589Cys
|
XM_011521971.2:c.1765C>T
(THBS1)
|
XP_011520273.1:p.Arg589Cys
|
XR_931897.1:n.2114C>T
(THBS1)
|
|