|
ENST00000348127.11:c.1671-3C>T
|
ENSP00000265385.8:n.1671-3C>T
|
|
|
ENST00000484496.6:n.1671-3C>T
|
|
|
|
ENST00000338791.11:c.1779-3C>T
MANE Select
|
ENSP00000345096.6:n.1779-3C>T
|
|
|
ENST00000648462.1:c.1428-3C>T
|
|
|
|
ENST00000338791.10:c.1779-3C>T
|
ENSP00000345096.6:n.1779-3C>T
|
|
|
ENST00000348127.10:c.1671-3C>T
|
ENSP00000265385.8:n.1671-3C>T
|
|
|
ENST00000354269.9:c.1749-3C>T
|
ENSP00000346219.5:n.1749-3C>T
|
|
|
ENST00000419067.6:c.1680-3C>T
|
ENSP00000399400.2:n.1680-3C>T
|
|
|
ENST00000469328.5:c.1544-3C>T
|
|
|
|
ENST00000470772.5:c.1521-3C>T
|
ENSP00000417296.1:n.1521-3C>T
|
|
|
ENST00000480861.5:c.1509-3C>T
|
ENSP00000420185.1:n.1509-3C>T
|
|
|
ENST00000484496.5:c.1671-3C>T
|
ENSP00000418742.1:n.1671-3C>T
|
|
|
ENST00000496200.5:c.1449-3C>T
|
ENSP00000420803.1:n.1449-3C>T
|
|
|
ENST00000626419.2:c.1521-3C>T
|
ENSP00000486056.1:n.1521-3C>T
|
|
|
NM_000883.3:c.1779-3C>T
|
NP_000874.2:n.1779-3C>T
|
|
|
NM_001102605.1:c.1749-3C>T
|
NP_001096075.1:n.1749-3C>T
|
|
|
NM_001142573.1:c.1524-3C>T
|
NP_001136045.1:n.1524-3C>T
|
|
|
NM_001142574.1:c.1509-3C>T
|
NP_001136046.1:n.1509-3C>T
|
|
|
NM_001142575.1:c.1449-3C>T
|
NP_001136047.1:n.1449-3C>T
|
|
|
NM_001142576.1:c.1680-3C>T
|
NP_001136048.1:n.1680-3C>T
|
|
|
NM_001304521.1:c.1572-3C>T
|
NP_001291450.1:n.1572-3C>T
|
|
|
NM_183243.2:c.1671-3C>T
|
NP_899066.1:n.1671-3C>T
|
|
|
XM_005250314.1:c.1548-3C>T
|
XP_005250371.1:n.1548-3C>T
|
|
|
XM_006715967.1:c.1796-3C>T
|
XP_006716030.1:n.1796-3C>T
|
|
|
XM_006715968.1:c.1766-3C>T
|
XP_006716031.1:n.1766-3C>T
|
|
|
XM_006715969.1:c.1688-3C>T
|
XP_006716032.1:n.1688-3C>T
|
|
|
XM_006715970.2:c.1589-3C>T
|
XP_006716033.1:n.1589-3C>T
|
|
|
XM_006715971.1:c.1565-3C>T
|
XP_006716034.1:n.1565-3C>T
|
|
|
XM_011516156.1:c.1178-3C>T
|
XP_011514458.1:n.1178-3C>T
|
|
|
XM_011516157.1:c.1161-3C>T
|
XP_011514459.1:n.1161-3C>T
|
|
|
XM_017012172.1:c.1548-3C>T
|
XP_016867661.1:n.1548-3C>T
|
|
|
XM_024446755.1:c.1766-3C>T
|
XP_024302523.1:n.1766-3C>T
|
|
|
XM_024446756.1:c.1688-3C>T
|
XP_024302524.1:n.1688-3C>T
|
|
|
XM_024446757.1:c.1589-3C>T
|
XP_024302525.1:n.1589-3C>T
|
|
|
XM_024446758.1:c.1565-3C>T
|
XP_024302526.1:n.1565-3C>T
|
|
|
NM_000883.4:c.1779-3C>T
MANE Select
|
NP_000874.2:n.1779-3C>T
|
|
|
NM_001102605.2:c.1749-3C>T
|
NP_001096075.1:n.1749-3C>T
|
|
|
NM_001142573.2:c.1524-3C>T
|
NP_001136045.1:n.1524-3C>T
|
|
|
NM_001142574.2:c.1509-3C>T
|
NP_001136046.1:n.1509-3C>T
|
|
|
NM_001142575.2:c.1449-3C>T
|
NP_001136047.1:n.1449-3C>T
|
|
|
NM_001142576.2:c.1680-3C>T
|
NP_001136048.1:n.1680-3C>T
|
|
|
NM_001304521.2:c.1572-3C>T
|
NP_001291450.1:n.1572-3C>T
|
|
|
NM_183243.3:c.1671-3C>T
|
NP_899066.1:n.1671-3C>T
|
|
