|
ENST00000356518.7:c.2405-112G>T
MANE Select
|
ENSP00000348912.3:n.2405-112G>T
|
|
|
ENST00000350009.6:c.2327-112G>T
|
ENSP00000322550.5:n.2327-112G>T
|
|
|
ENST00000356518.6:c.2405-112G>T
|
ENSP00000348912.2:n.2405-112G>T
|
|
|
ENST00000379861.8:c.2405-115G>T
|
ENSP00000369190.4:n.2405-115G>T
|
|
|
ENST00000466620.5:n.1966-112G>T
|
|
|
|
ENST00000483362.1:n.1328-112G>T
|
|
|
|
ENST00000617732.1:c.*1092-115G>T
|
ENSP00000483343.1:n.*1092-115G>T
|
|
|
ENST00000619289.4:c.2045-115G>T
|
ENSP00000484600.1:n.2045-115G>T
|
|
|
NM_001282447.1:c.2405-115G>T
|
NP_001269376.1:n.2405-115G>T
|
|
|
NM_025220.3:c.2405-112G>T
|
NP_079496.1:n.2405-112G>T
|
|
|
NM_153202.2:c.2327-112G>T
|
NP_694882.1:n.2327-112G>T
|
|
|
XM_005260843.1:c.2444-112G>T
|
XP_005260900.1:n.2444-112G>T
|
|
|
XM_006723639.1:c.2444-115G>T
|
XP_006723702.1:n.2444-115G>T
|
|
|
XM_006723640.1:c.2435-112G>T
|
XP_006723703.1:n.2435-112G>T
|
|
|
XM_011529366.1:c.2441-112G>T
|
XP_011527668.1:n.2441-112G>T
|
|
|
XM_011529367.1:c.2402-112G>T
|
XP_011527669.1:n.2402-112G>T
|
|
|
XM_011529368.1:c.2366-112G>T
|
XP_011527670.1:n.2366-112G>T
|
|
|
XM_011529373.1:c.1442-112G>T
|
XP_011527675.1:n.1442-112G>T
|
|
|
XR_937151.1:n.2456-112G>T
|
|
|
|
XR_937152.1:n.2456-115G>T
|
|
|
|
XR_937153.1:n.2429-115G>T
|
|
|
|
XR_937154.1:n.2429-115G>T
|
|
|
|
XR_937155.1:n.2350-115G>T
|
|
|
|
XR_937157.1:n.2352-115G>T
|
|
|
|
NM_001282447.2:c.2405-115G>T
|
NP_001269376.1:n.2405-115G>T
|
|
|
NM_025220.4:c.2405-112G>T
|
NP_079496.1:n.2405-112G>T
|
|
|
NM_153202.3:c.2327-112G>T
|
NP_694882.1:n.2327-112G>T
|
|
|
XM_011529373.2:c.1442-112G>T
|
XP_011527675.1:n.1442-112G>T
|
|
|
XR_001754405.1:n.2516-115G>T
|
|
|
|
XR_002958534.1:n.2625-115G>T
|
|
|
|
NM_001282447.3:c.2405-115G>T
|
NP_001269376.1:n.2405-115G>T
|
|
|
NM_025220.5:c.2405-112G>T
MANE Select
|
NP_079496.1:n.2405-112G>T
|
|
|
NM_153202.4:c.2327-112G>T
|
NP_694882.1:n.2327-112G>T
|
|
