ENST00000681993.1:n.597G>A
|
|
|
ENST00000682295.1:c.303+128G>A
|
ENSP00000507499.1:n.303+128G>A
|
|
ENST00000682303.1:c.*2831G>A
|
ENSP00000508325.1:n.*2831G>A
|
|
ENST00000682308.1:c.3045G>A
|
ENSP00000507056.1:p.Trp1015Ter
|
|
ENST00000682480.1:c.3063G>A
|
ENSP00000508344.1:p.Trp1021Ter
|
|
ENST00000682546.1:c.3042G>A
|
ENSP00000508188.1:p.Trp1014Ter
|
|
ENST00000682585.1:c.3045G>A
|
ENSP00000506885.1:p.Trp1015Ter
|
|
ENST00000682595.1:n.3629G>A
|
|
|
ENST00000682607.1:c.1463G>A
|
|
|
ENST00000682779.1:c.3036G>A
|
ENSP00000507947.1:p.Trp1012Ter
|
|
ENST00000682845.1:n.2147G>A
|
|
|
ENST00000682885.1:c.3000G>A
|
ENSP00000508036.1:p.Trp1000Ter
|
|
ENST00000682933.1:n.3119G>A
|
|
|
ENST00000683072.1:n.3629G>A
|
|
|
ENST00000683080.1:n.664G>A
|
|
|
ENST00000683125.1:c.3153G>A
|
ENSP00000507939.1:p.Trp1051Ter
|
|
ENST00000683213.1:c.3048G>A
|
ENSP00000507751.1:p.Trp1016Ter
|
|
ENST00000683220.1:c.3075G>A
|
ENSP00000507151.1:p.Trp1025Ter
|
|
ENST00000683329.1:n.3848G>A
|
|
|
ENST00000683346.1:c.*2920G>A
|
ENSP00000507458.1:n.*2920G>A
|
|
ENST00000683409.1:n.1652G>A
|
|
|
ENST00000683459.1:n.3632G>A
|
|
|
ENST00000683590.1:c.2897-5570G>A
|
ENSP00000506820.1:n.2897-5570G>A
|
|
ENST00000683623.1:c.2952G>A
|
ENSP00000507702.1:p.Trp984Ter
|
|
ENST00000683645.1:n.3596G>A
|
|
|
ENST00000683796.1:c.*2917G>A
|
ENSP00000508221.1:n.*2917G>A
|
|
ENST00000683802.1:n.5970G>A
|
|
|
ENST00000683833.1:c.3036G>A
|
ENSP00000506852.1:p.Trp1012Ter
|
|
ENST00000683994.1:c.3045G>A
|
ENSP00000507181.1:p.Trp1015Ter
|
|
ENST00000684290.1:c.*581G>A
|
ENSP00000507243.1:n.*581G>A
|
|
ENST00000684306.1:c.*2958G>A
|
ENSP00000508384.1:n.*2958G>A
|
|
ENST00000684341.1:n.3065G>A
|
|
|
ENST00000684383.1:c.*2683G>A
|
ENSP00000506863.1:n.*2683G>A
|
|
ENST00000684619.1:c.*2917G>A
|
ENSP00000508088.1:n.*2917G>A
|
|
ENST00000684705.1:n.166G>A
|
|
|
ENST00000684743.1:n.4076G>A
|
|
|
ENST00000260665.12:c.3045G>A
MANE Select
|
ENSP00000260665.7:p.Trp1015Ter
|
|
ENST00000260665.11:c.3045G>A
|
ENSP00000260665.7:p.Trp1015Ter
|
|
NM_133259.3:c.3045G>A
|
NP_573566.2:p.Trp1015Ter
|
|
XM_006711915.2:c.2967G>A
|
XP_006711978.1:p.Trp989Ter
|
|
XM_006711916.2:c.3045G>A
|
XP_006711979.1:p.Trp1015Ter
|
|
XM_011532473.1:c.3045G>A
|
XP_011530775.1:p.Trp1015Ter
|
|
XM_011532474.1:c.3045G>A
|
XP_011530776.1:p.Trp1015Ter
|
|
XM_006711916.3:c.3045G>A
|
XP_006711979.1:p.Trp1015Ter
|
|
XM_017003117.1:c.2967G>A
|
XP_016858606.1:p.Trp989Ter
|
|
XR_002958896.1:n.3087G>A
|
|
|
NM_133259.4:c.3045G>A
MANE Select
|
NP_573566.2:p.Trp1015Ter
|
|