ENST00000472420.6:n.373G>A
|
|
|
ENST00000681993.1:n.846G>A
|
|
|
ENST00000682295.1:c.449G>A
|
ENSP00000507499.1:n.449G>A
|
|
ENST00000682303.1:c.*3080G>A
|
ENSP00000508325.1:n.*3080G>A
|
|
ENST00000682308.1:c.3294G>A
|
ENSP00000507056.1:p.Lys1098=
|
|
ENST00000682480.1:c.3312G>A
|
ENSP00000508344.1:p.Lys1104=
|
|
ENST00000682546.1:c.3291G>A
|
ENSP00000508188.1:p.Lys1097=
|
|
ENST00000682585.1:c.3294G>A
|
ENSP00000506885.1:p.Lys1098=
|
|
ENST00000682595.1:n.3878G>A
|
|
|
ENST00000682607.1:c.1712G>A
|
|
|
ENST00000682612.1:c.146G>A
|
|
|
ENST00000682779.1:c.3285G>A
|
ENSP00000507947.1:p.Lys1095=
|
|
ENST00000682845.1:n.2396G>A
|
|
|
ENST00000682885.1:c.3249G>A
|
ENSP00000508036.1:p.Lys1083=
|
|
ENST00000682933.1:n.3368G>A
|
|
|
ENST00000683002.1:c.146G>A
|
|
|
ENST00000683072.1:n.3878G>A
|
|
|
ENST00000683080.1:n.913G>A
|
|
|
ENST00000683125.1:c.3402G>A
|
ENSP00000507939.1:p.Lys1134=
|
|
ENST00000683213.1:c.3297G>A
|
ENSP00000507751.1:p.Lys1099=
|
|
ENST00000683220.1:c.3324G>A
|
ENSP00000507151.1:p.Lys1108=
|
|
ENST00000683329.1:n.4097G>A
|
|
|
ENST00000683346.1:c.*3169G>A
|
ENSP00000507458.1:n.*3169G>A
|
|
ENST00000683409.1:n.1901G>A
|
|
|
ENST00000683459.1:n.3881G>A
|
|
|
ENST00000683528.1:c.146G>A
|
|
|
ENST00000683590.1:c.3042G>A
|
ENSP00000506820.1:p.Lys1014=
|
|
ENST00000683623.1:c.3201G>A
|
ENSP00000507702.1:p.Lys1067=
|
|
ENST00000683645.1:n.3845G>A
|
|
|
ENST00000683796.1:c.*3166G>A
|
ENSP00000508221.1:n.*3166G>A
|
|
ENST00000683802.1:n.6219G>A
|
|
|
ENST00000683833.1:c.3285G>A
|
ENSP00000506852.1:p.Lys1095=
|
|
ENST00000683994.1:c.3294G>A
|
ENSP00000507181.1:p.Lys1098=
|
|
ENST00000684290.1:c.*830G>A
|
ENSP00000507243.1:n.*830G>A
|
|
ENST00000684306.1:c.*3207G>A
|
ENSP00000508384.1:n.*3207G>A
|
|
ENST00000684341.1:n.3314G>A
|
|
|
ENST00000684383.1:c.*2932G>A
|
ENSP00000506863.1:n.*2932G>A
|
|
ENST00000684418.1:n.4475G>A
|
|
|
ENST00000684454.1:n.2644G>A
|
|
|
ENST00000684619.1:c.*3166G>A
|
ENSP00000508088.1:n.*3166G>A
|
|
ENST00000684743.1:n.4325G>A
|
|
|
ENST00000260665.12:c.3294G>A
MANE Select
|
ENSP00000260665.7:p.Lys1098=
|
|
ENST00000260665.11:c.3294G>A
|
ENSP00000260665.7:p.Lys1098=
|
|
NM_133259.3:c.3294G>A
|
NP_573566.2:p.Lys1098=
|
|
XM_006711915.2:c.3216G>A
|
XP_006711978.1:p.Lys1072=
|
|
XM_011532473.1:c.3294G>A
|
XP_011530775.1:p.Lys1098=
|
|
XM_011532474.1:c.3294G>A
|
XP_011530776.1:p.Lys1098=
|
|
XM_017003117.1:c.3216G>A
|
XP_016858606.1:p.Lys1072=
|
|
XR_002958896.1:n.3336G>A
|
|
|
NM_133259.4:c.3294G>A
MANE Select
|
NP_573566.2:p.Lys1098=
|
|