ENST00000681993.1:n.605A>G
|
|
|
ENST00000682295.1:c.303+136A>G
|
ENSP00000507499.1:n.303+136A>G
|
|
ENST00000682303.1:c.*2839A>G
|
ENSP00000508325.1:n.*2839A>G
|
|
ENST00000682308.1:c.3053A>G
|
ENSP00000507056.1:p.Asp1018Gly
|
|
ENST00000682480.1:c.3071A>G
|
ENSP00000508344.1:p.Asp1024Gly
|
|
ENST00000682546.1:c.3050A>G
|
ENSP00000508188.1:p.Asp1017Gly
|
|
ENST00000682585.1:c.3053A>G
|
ENSP00000506885.1:p.Asp1018Gly
|
|
ENST00000682595.1:n.3637A>G
|
|
|
ENST00000682607.1:c.1471A>G
|
|
|
ENST00000682779.1:c.3044A>G
|
ENSP00000507947.1:p.Asp1015Gly
|
|
ENST00000682845.1:n.2155A>G
|
|
|
ENST00000682885.1:c.3008A>G
|
ENSP00000508036.1:p.Asp1003Gly
|
|
ENST00000682933.1:n.3127A>G
|
|
|
ENST00000683072.1:n.3637A>G
|
|
|
ENST00000683080.1:n.672A>G
|
|
|
ENST00000683125.1:c.3161A>G
|
ENSP00000507939.1:p.Asp1054Gly
|
|
ENST00000683213.1:c.3056A>G
|
ENSP00000507751.1:p.Asp1019Gly
|
|
ENST00000683220.1:c.3083A>G
|
ENSP00000507151.1:p.Asp1028Gly
|
|
ENST00000683329.1:n.3856A>G
|
|
|
ENST00000683346.1:c.*2928A>G
|
ENSP00000507458.1:n.*2928A>G
|
|
ENST00000683409.1:n.1660A>G
|
|
|
ENST00000683459.1:n.3640A>G
|
|
|
ENST00000683590.1:c.2897-5562A>G
|
ENSP00000506820.1:n.2897-5562A>G
|
|
ENST00000683623.1:c.2960A>G
|
ENSP00000507702.1:p.Asp987Gly
|
|
ENST00000683645.1:n.3604A>G
|
|
|
ENST00000683796.1:c.*2925A>G
|
ENSP00000508221.1:n.*2925A>G
|
|
ENST00000683802.1:n.5978A>G
|
|
|
ENST00000683833.1:c.3044A>G
|
ENSP00000506852.1:p.Asp1015Gly
|
|
ENST00000683994.1:c.3053A>G
|
ENSP00000507181.1:p.Asp1018Gly
|
|
ENST00000684290.1:c.*589A>G
|
ENSP00000507243.1:n.*589A>G
|
|
ENST00000684306.1:c.*2966A>G
|
ENSP00000508384.1:n.*2966A>G
|
|
ENST00000684341.1:n.3073A>G
|
|
|
ENST00000684383.1:c.*2691A>G
|
ENSP00000506863.1:n.*2691A>G
|
|
ENST00000684619.1:c.*2925A>G
|
ENSP00000508088.1:n.*2925A>G
|
|
ENST00000684705.1:n.174A>G
|
|
|
ENST00000684743.1:n.4084A>G
|
|
|
ENST00000260665.12:c.3053A>G
MANE Select
|
ENSP00000260665.7:p.Asp1018Gly
|
|
ENST00000260665.11:c.3053A>G
|
ENSP00000260665.7:p.Asp1018Gly
|
|
NM_133259.3:c.3053A>G
|
NP_573566.2:p.Asp1018Gly
|
|
XM_006711915.2:c.2975A>G
|
XP_006711978.1:p.Asp992Gly
|
|
XM_006711916.2:c.3053A>G
|
XP_006711979.1:p.Asp1018Gly
|
|
XM_011532473.1:c.3053A>G
|
XP_011530775.1:p.Asp1018Gly
|
|
XM_011532474.1:c.3053A>G
|
XP_011530776.1:p.Asp1018Gly
|
|
XM_006711916.3:c.3053A>G
|
XP_006711979.1:p.Asp1018Gly
|
|
XM_017003117.1:c.2975A>G
|
XP_016858606.1:p.Asp992Gly
|
|
XR_002958896.1:n.3095A>G
|
|
|
NM_133259.4:c.3053A>G
MANE Select
|
NP_573566.2:p.Asp1018Gly
|
|