ENST00000472420.6:n.363C>G
|
|
|
ENST00000681993.1:n.836C>G
|
|
|
ENST00000682295.1:c.439C>G
|
ENSP00000507499.1:n.439C>G
|
|
ENST00000682303.1:c.*3070C>G
|
ENSP00000508325.1:n.*3070C>G
|
|
ENST00000682308.1:c.3284C>G
|
ENSP00000507056.1:p.Thr1095Ser
|
|
ENST00000682480.1:c.3302C>G
|
ENSP00000508344.1:p.Thr1101Ser
|
|
ENST00000682546.1:c.3281C>G
|
ENSP00000508188.1:p.Thr1094Ser
|
|
ENST00000682585.1:c.3284C>G
|
ENSP00000506885.1:p.Thr1095Ser
|
|
ENST00000682595.1:n.3868C>G
|
|
|
ENST00000682607.1:c.1702C>G
|
|
|
ENST00000682612.1:c.136C>G
|
|
|
ENST00000682779.1:c.3275C>G
|
ENSP00000507947.1:p.Thr1092Ser
|
|
ENST00000682845.1:n.2386C>G
|
|
|
ENST00000682885.1:c.3239C>G
|
ENSP00000508036.1:p.Thr1080Ser
|
|
ENST00000682933.1:n.3358C>G
|
|
|
ENST00000683002.1:c.136C>G
|
|
|
ENST00000683072.1:n.3868C>G
|
|
|
ENST00000683080.1:n.903C>G
|
|
|
ENST00000683125.1:c.3392C>G
|
ENSP00000507939.1:p.Thr1131Ser
|
|
ENST00000683213.1:c.3287C>G
|
ENSP00000507751.1:p.Thr1096Ser
|
|
ENST00000683220.1:c.3314C>G
|
ENSP00000507151.1:p.Thr1105Ser
|
|
ENST00000683329.1:n.4087C>G
|
|
|
ENST00000683346.1:c.*3159C>G
|
ENSP00000507458.1:n.*3159C>G
|
|
ENST00000683409.1:n.1891C>G
|
|
|
ENST00000683459.1:n.3871C>G
|
|
|
ENST00000683528.1:c.136C>G
|
|
|
ENST00000683590.1:c.3032C>G
|
ENSP00000506820.1:p.Thr1011Ser
|
|
ENST00000683623.1:c.3191C>G
|
ENSP00000507702.1:p.Thr1064Ser
|
|
ENST00000683645.1:n.3835C>G
|
|
|
ENST00000683796.1:c.*3156C>G
|
ENSP00000508221.1:n.*3156C>G
|
|
ENST00000683802.1:n.6209C>G
|
|
|
ENST00000683833.1:c.3275C>G
|
ENSP00000506852.1:p.Thr1092Ser
|
|
ENST00000683994.1:c.3284C>G
|
ENSP00000507181.1:p.Thr1095Ser
|
|
ENST00000684290.1:c.*820C>G
|
ENSP00000507243.1:n.*820C>G
|
|
ENST00000684306.1:c.*3197C>G
|
ENSP00000508384.1:n.*3197C>G
|
|
ENST00000684341.1:n.3304C>G
|
|
|
ENST00000684383.1:c.*2922C>G
|
ENSP00000506863.1:n.*2922C>G
|
|
ENST00000684418.1:n.4465C>G
|
|
|
ENST00000684454.1:n.2634C>G
|
|
|
ENST00000684619.1:c.*3156C>G
|
ENSP00000508088.1:n.*3156C>G
|
|
ENST00000684743.1:n.4315C>G
|
|
|
ENST00000260665.12:c.3284C>G
MANE Select
|
ENSP00000260665.7:p.Thr1095Ser
|
|
ENST00000260665.11:c.3284C>G
|
ENSP00000260665.7:p.Thr1095Ser
|
|
NM_133259.3:c.3284C>G
|
NP_573566.2:p.Thr1095Ser
|
|
XM_006711915.2:c.3206C>G
|
XP_006711978.1:p.Thr1069Ser
|
|
XM_011532473.1:c.3284C>G
|
XP_011530775.1:p.Thr1095Ser
|
|
XM_011532474.1:c.3284C>G
|
XP_011530776.1:p.Thr1095Ser
|
|
XM_017003117.1:c.3206C>G
|
XP_016858606.1:p.Thr1069Ser
|
|
XR_002958896.1:n.3326C>G
|
|
|
NM_133259.4:c.3284C>G
MANE Select
|
NP_573566.2:p.Thr1095Ser
|
|