ENST00000681993.1:n.664G>C
|
|
|
ENST00000682295.1:c.303+195G>C
|
ENSP00000507499.1:n.303+195G>C
|
|
ENST00000682303.1:c.*2898G>C
|
ENSP00000508325.1:n.*2898G>C
|
|
ENST00000682308.1:c.3112G>C
|
ENSP00000507056.1:p.Asp1038His
|
|
ENST00000682480.1:c.3130G>C
|
ENSP00000508344.1:p.Asp1044His
|
|
ENST00000682546.1:c.3109G>C
|
ENSP00000508188.1:p.Asp1037His
|
|
ENST00000682585.1:c.3112G>C
|
ENSP00000506885.1:p.Asp1038His
|
|
ENST00000682595.1:n.3696G>C
|
|
|
ENST00000682607.1:c.1530G>C
|
|
|
ENST00000682779.1:c.3103G>C
|
ENSP00000507947.1:p.Asp1035His
|
|
ENST00000682845.1:n.2214G>C
|
|
|
ENST00000682885.1:c.3067G>C
|
ENSP00000508036.1:p.Asp1023His
|
|
ENST00000682933.1:n.3186G>C
|
|
|
ENST00000683072.1:n.3696G>C
|
|
|
ENST00000683080.1:n.731G>C
|
|
|
ENST00000683125.1:c.3220G>C
|
ENSP00000507939.1:p.Asp1074His
|
|
ENST00000683213.1:c.3115G>C
|
ENSP00000507751.1:p.Asp1039His
|
|
ENST00000683220.1:c.3142G>C
|
ENSP00000507151.1:p.Asp1048His
|
|
ENST00000683329.1:n.3915G>C
|
|
|
ENST00000683346.1:c.*2987G>C
|
ENSP00000507458.1:n.*2987G>C
|
|
ENST00000683409.1:n.1719G>C
|
|
|
ENST00000683459.1:n.3699G>C
|
|
|
ENST00000683590.1:c.2897-5503G>C
|
ENSP00000506820.1:n.2897-5503G>C
|
|
ENST00000683623.1:c.3019G>C
|
ENSP00000507702.1:p.Asp1007His
|
|
ENST00000683645.1:n.3663G>C
|
|
|
ENST00000683796.1:c.*2984G>C
|
ENSP00000508221.1:n.*2984G>C
|
|
ENST00000683802.1:n.6037G>C
|
|
|
ENST00000683833.1:c.3103G>C
|
ENSP00000506852.1:p.Asp1035His
|
|
ENST00000683994.1:c.3112G>C
|
ENSP00000507181.1:p.Asp1038His
|
|
ENST00000684290.1:c.*648G>C
|
ENSP00000507243.1:n.*648G>C
|
|
ENST00000684306.1:c.*3025G>C
|
ENSP00000508384.1:n.*3025G>C
|
|
ENST00000684341.1:n.3132G>C
|
|
|
ENST00000684383.1:c.*2750G>C
|
ENSP00000506863.1:n.*2750G>C
|
|
ENST00000684619.1:c.*2984G>C
|
ENSP00000508088.1:n.*2984G>C
|
|
ENST00000684705.1:n.233G>C
|
|
|
ENST00000684743.1:n.4143G>C
|
|
|
ENST00000260665.12:c.3112G>C
MANE Select
|
ENSP00000260665.7:p.Asp1038His
|
|
ENST00000260665.11:c.3112G>C
|
ENSP00000260665.7:p.Asp1038His
|
|
NM_133259.3:c.3112G>C
|
NP_573566.2:p.Asp1038His
|
|
XM_006711915.2:c.3034G>C
|
XP_006711978.1:p.Asp1012His
|
|
XM_006711916.2:c.3112G>C
|
XP_006711979.1:p.Asp1038His
|
|
XM_011532473.1:c.3112G>C
|
XP_011530775.1:p.Asp1038His
|
|
XM_011532474.1:c.3112G>C
|
XP_011530776.1:p.Asp1038His
|
|
XM_006711916.3:c.3112G>C
|
XP_006711979.1:p.Asp1038His
|
|
XM_017003117.1:c.3034G>C
|
XP_016858606.1:p.Asp1012His
|
|
XR_002958896.1:n.3154G>C
|
|
|
NM_133259.4:c.3112G>C
MANE Select
|
NP_573566.2:p.Asp1038His
|
|