|
ENST00000328664.9:c.635-3C>T
(RHD)
MANE Select
|
ENSP00000331871.4:n.635-3C>T
|
|
|
ENST00000648012.1:c.635-3C>T
(RHD)
|
ENSP00000498055.1:n.635-3C>T
|
|
|
ENST00000328664.8:c.635-3C>T
(RHD)
|
ENSP00000331871.4:n.635-3C>T
|
|
|
ENST00000342055.9:c.635-3C>T
(RHD)
|
ENSP00000339577.5:n.635-3C>T
|
|
|
ENST00000357542.8:c.635-3C>T
(RHD)
|
ENSP00000350150.4:n.635-3C>T
|
|
|
ENST00000417538.6:c.635-3C>T
(RHD)
|
ENSP00000396420.2:n.635-3C>T
|
|
|
ENST00000423253.1:n.635-3C>T
(RHD)
|
|
|
|
ENST00000423810.6:c.635-3C>T
(RHD)
|
ENSP00000399640.2:n.635-3C>T
|
|
|
ENST00000454452.6:c.635-3C>T
(RHD)
|
ENSP00000413849.2:n.635-3C>T
|
|
|
ENST00000473314.6:c.-67+35523G>A
(RSRP1)
|
ENSP00000457582.1:n.-67+35523G>A
|
|
|
ENST00000561867.1:c.-67+36461G>A
(RSRP1)
|
ENSP00000456995.1:n.-67+36461G>A
|
|
|
ENST00000564398.5:n.790-3C>T
(RHD)
|
|
|
|
ENST00000568195.5:c.635-3C>T
(RHD)
|
ENSP00000456966.1:n.635-3C>T
|
|
|
ENST00000568996.1:c.-67+36552G>A
(RSRP1)
|
ENSP00000458042.1:n.-67+36552G>A
|
|
|
ENST00000615607.1:c.635-3C>T
(RHD)
|
ENSP00000480925.1:n.635-3C>T
|
|
|
ENST00000622561.4:c.635-3C>T
(RHD)
|
ENSP00000478087.1:n.635-3C>T
|
|
|
NM_001127691.2:c.635-3C>T
(RHD)
|
NP_001121163.1:n.635-3C>T
|
|
|
NM_001282867.1:c.137-3C>T
(RHD)
|
NP_001269796.1:n.137-3C>T
|
|
|
NM_001282868.1:c.635-3C>T
(RHD)
|
NP_001269797.1:n.635-3C>T
|
|
|
NM_001282869.1:c.635-3C>T
(RHD)
|
NP_001269798.1:n.635-3C>T
|
|
|
NM_001282870.1:c.635-3C>T
(RHD)
|
NP_001269799.1:n.635-3C>T
|
|
|
NM_001282871.1:c.635-3C>T
(RHD)
|
NP_001269800.1:n.635-3C>T
|
|
|
NM_001282872.1:c.635-3C>T
(RHD)
|
NP_001269801.1:n.635-3C>T
|
|
|
NM_016124.4:c.635-3C>T
(RHD)
|
NP_057208.2:n.635-3C>T
|
|
|
XM_011541892.1:c.635-3C>T
(RHD)
|
XP_011540194.1:n.635-3C>T
|
|
|
XR_946734.1:n.790-3C>T
(RHD)
|
|
|
|
XR_946735.1:n.790-3C>T
(RHD)
|
|
|
|
XR_946736.1:n.790-3C>T
(RHD)
|
|
|
|
XR_946737.1:n.790-3C>T
(RHD)
|
|
|
|
XR_947098.1:n.144-9749G>A
|
|
|
|
NM_001321772.1:c.-67+35523G>A
(RSRP1)
|
NP_001308701.1:n.-67+35523G>A
|
|
|
NR_135787.1:n.1215+35523G>A
(RSRP1)
|
|
|
|
NR_135788.1:n.277+36461G>A
(RSRP1)
|
|
|
|
NR_135789.1:n.1215+35523G>A
(RSRP1)
|
|
|
|
XM_017002015.1:c.635-3C>T
(RHD)
|
XP_016857504.1:n.635-3C>T
|
|
|
XR_946737.2:n.790-3C>T
(RHD)
|
|
|
|
NM_001127691.3:c.635-3C>T
(RHD)
|
NP_001121163.1:n.635-3C>T
|
|
|
NM_001282869.2:c.635-3C>T
(RHD)
|
NP_001269798.1:n.635-3C>T
|
|
|
NM_001282871.2:c.635-3C>T
(RHD)
|
NP_001269800.1:n.635-3C>T
|
|
|
NM_001321772.2:c.-67+35523G>A
(RSRP1)
|
NP_001308701.1:n.-67+35523G>A
|
|
|
NM_016124.5:c.-4294966622-3C>T
|
|
|
|
NR_135787.2:n.1215+35523G>A
(RSRP1)
|
|
|
|
NR_135788.2:n.277+36461G>A
(RSRP1)
|
|
|
|
NR_135789.2:n.1215+35523G>A
(RSRP1)
|
|
|
|
NM_016124.6:c.635-3C>T
(RHD)
MANE Select
|
NP_057208.3:n.635-3C>T
|
|
