ENST00000681993.1:n.653A>G
|
|
|
ENST00000682295.1:c.303+184A>G
|
ENSP00000507499.1:n.303+184A>G
|
|
ENST00000682303.1:c.*2887A>G
|
ENSP00000508325.1:n.*2887A>G
|
|
ENST00000682308.1:c.3101A>G
|
ENSP00000507056.1:p.Asp1034Gly
|
|
ENST00000682480.1:c.3119A>G
|
ENSP00000508344.1:p.Asp1040Gly
|
|
ENST00000682546.1:c.3098A>G
|
ENSP00000508188.1:p.Asp1033Gly
|
|
ENST00000682585.1:c.3101A>G
|
ENSP00000506885.1:p.Asp1034Gly
|
|
ENST00000682595.1:n.3685A>G
|
|
|
ENST00000682607.1:c.1519A>G
|
|
|
ENST00000682779.1:c.3092A>G
|
ENSP00000507947.1:p.Asp1031Gly
|
|
ENST00000682845.1:n.2203A>G
|
|
|
ENST00000682885.1:c.3056A>G
|
ENSP00000508036.1:p.Asp1019Gly
|
|
ENST00000682933.1:n.3175A>G
|
|
|
ENST00000683072.1:n.3685A>G
|
|
|
ENST00000683080.1:n.720A>G
|
|
|
ENST00000683125.1:c.3209A>G
|
ENSP00000507939.1:p.Asp1070Gly
|
|
ENST00000683213.1:c.3104A>G
|
ENSP00000507751.1:p.Asp1035Gly
|
|
ENST00000683220.1:c.3131A>G
|
ENSP00000507151.1:p.Asp1044Gly
|
|
ENST00000683329.1:n.3904A>G
|
|
|
ENST00000683346.1:c.*2976A>G
|
ENSP00000507458.1:n.*2976A>G
|
|
ENST00000683409.1:n.1708A>G
|
|
|
ENST00000683459.1:n.3688A>G
|
|
|
ENST00000683590.1:c.2897-5514A>G
|
ENSP00000506820.1:n.2897-5514A>G
|
|
ENST00000683623.1:c.3008A>G
|
ENSP00000507702.1:p.Asp1003Gly
|
|
ENST00000683645.1:n.3652A>G
|
|
|
ENST00000683796.1:c.*2973A>G
|
ENSP00000508221.1:n.*2973A>G
|
|
ENST00000683802.1:n.6026A>G
|
|
|
ENST00000683833.1:c.3092A>G
|
ENSP00000506852.1:p.Asp1031Gly
|
|
ENST00000683994.1:c.3101A>G
|
ENSP00000507181.1:p.Asp1034Gly
|
|
ENST00000684290.1:c.*637A>G
|
ENSP00000507243.1:n.*637A>G
|
|
ENST00000684306.1:c.*3014A>G
|
ENSP00000508384.1:n.*3014A>G
|
|
ENST00000684341.1:n.3121A>G
|
|
|
ENST00000684383.1:c.*2739A>G
|
ENSP00000506863.1:n.*2739A>G
|
|
ENST00000684619.1:c.*2973A>G
|
ENSP00000508088.1:n.*2973A>G
|
|
ENST00000684705.1:n.222A>G
|
|
|
ENST00000684743.1:n.4132A>G
|
|
|
ENST00000260665.12:c.3101A>G
MANE Select
|
ENSP00000260665.7:p.Asp1034Gly
|
|
ENST00000260665.11:c.3101A>G
|
ENSP00000260665.7:p.Asp1034Gly
|
|
NM_133259.3:c.3101A>G
|
NP_573566.2:p.Asp1034Gly
|
|
XM_006711915.2:c.3023A>G
|
XP_006711978.1:p.Asp1008Gly
|
|
XM_006711916.2:c.3101A>G
|
XP_006711979.1:p.Asp1034Gly
|
|
XM_011532473.1:c.3101A>G
|
XP_011530775.1:p.Asp1034Gly
|
|
XM_011532474.1:c.3101A>G
|
XP_011530776.1:p.Asp1034Gly
|
|
XM_006711916.3:c.3101A>G
|
XP_006711979.1:p.Asp1034Gly
|
|
XM_017003117.1:c.3023A>G
|
XP_016858606.1:p.Asp1008Gly
|
|
XR_002958896.1:n.3143A>G
|
|
|
NM_133259.4:c.3101A>G
MANE Select
|
NP_573566.2:p.Asp1034Gly
|
|