ENST00000266085.7:c.*506G>A
(TIMP3)
MANE Select
|
ENSP00000266085.5:n.*506G>A
|
|
ENST00000358763.7:c.711+5032C>T
(SYN3)
MANE Select
|
ENSP00000351614.2:n.711+5032C>T
|
|
ENST00000266085.6:c.*506G>A
(TIMP3)
|
ENSP00000266085.5:n.*506G>A
|
|
ENST00000358763.6:c.711+5032C>T
(SYN3)
|
ENSP00000351614.2:n.711+5032C>T
|
|
ENST00000462268.1:n.225+5032C>T
(SYN3)
|
|
|
NM_000362.4:c.*506G>A
(TIMP3)
|
NP_000353.1:n.*506G>A
|
|
NM_001135774.1:c.708+5032C>T
(SYN3)
|
NP_001129246.1:n.708+5032C>T
|
|
NM_003490.3:c.711+5032C>T
(SYN3)
|
NP_003481.3:n.711+5032C>T
|
|
NM_133633.2:c.711+5032C>T
(SYN3)
|
NP_598344.2:n.711+5032C>T
|
|
XM_011530405.1:c.711+5032C>T
(SYN3)
|
XP_011528707.1:n.711+5032C>T
|
|
XM_011530406.1:c.711+5032C>T
(SYN3)
|
XP_011528708.1:n.711+5032C>T
|
|
XM_011530407.1:c.711+5032C>T
(SYN3)
|
XP_011528709.1:n.711+5032C>T
|
|
XM_011530408.1:c.711+5032C>T
(SYN3)
|
XP_011528710.1:n.711+5032C>T
|
|
XM_011530409.1:c.711+5032C>T
(SYN3)
|
XP_011528711.1:n.711+5032C>T
|
|
XM_011530410.1:c.357+5032C>T
(SYN3)
|
XP_011528712.1:n.357+5032C>T
|
|
XM_011530411.1:c.711+5032C>T
(SYN3)
|
XP_011528713.1:n.711+5032C>T
|
|
XM_011530413.1:c.711+5032C>T
(SYN3)
|
XP_011528715.1:n.711+5032C>T
|
|
XM_011530414.1:c.711+5032C>T
(SYN3)
|
XP_011528716.1:n.711+5032C>T
|
|
XR_937927.1:n.1195+5032C>T
(SYN3)
|
|
|
XM_011530405.3:c.711+5032C>T
(SYN3)
|
XP_011528707.1:n.711+5032C>T
|
|
XM_011530406.3:c.711+5032C>T
(SYN3)
|
XP_011528708.1:n.711+5032C>T
|
|
XM_011530407.3:c.711+5032C>T
(SYN3)
|
XP_011528709.1:n.711+5032C>T
|
|
XM_011530408.2:c.711+5032C>T
(SYN3)
|
XP_011528710.1:n.711+5032C>T
|
|
XM_011530410.3:c.357+5032C>T
(SYN3)
|
XP_011528712.1:n.357+5032C>T
|
|
XM_017028961.2:c.711+5032C>T
(SYN3)
|
XP_016884450.1:n.711+5032C>T
|
|
XM_017028962.2:c.711+5032C>T
(SYN3)
|
XP_016884451.1:n.711+5032C>T
|
|
XM_017028963.2:c.711+5032C>T
(SYN3)
|
XP_016884452.1:n.711+5032C>T
|
|
XM_017028964.2:c.708+5032C>T
(SYN3)
|
XP_016884453.1:n.708+5032C>T
|
|
XR_001755317.2:n.948+5032C>T
(SYN3)
|
|
|
NM_000362.5:c.*506G>A
(TIMP3)
MANE Select
|
NP_000353.1:n.*506G>A
|
|
NM_001135774.2:c.708+5032C>T
(SYN3)
|
NP_001129246.1:n.708+5032C>T
|
|
NM_001369907.1:c.711+5032C>T
(SYN3)
|
NP_001356836.1:n.711+5032C>T
|
|
NM_001369908.1:c.711+5032C>T
(SYN3)
|
NP_001356837.1:n.711+5032C>T
|
|
NM_001369909.1:c.708+5032C>T
(SYN3)
|
NP_001356838.1:n.708+5032C>T
|
|
NM_001369910.1:c.708+5032C>T
(SYN3)
|
NP_001356839.1:n.708+5032C>T
|
|
NM_003490.4:c.711+5032C>T
(SYN3)
MANE Select
|
NP_003481.3:n.711+5032C>T
|
|
NM_133633.3:c.711+5032C>T
(SYN3)
|
NP_598344.2:n.711+5032C>T
|
|