ENST00000681993.1:n.627T>G
|
|
|
ENST00000682295.1:c.303+158T>G
|
ENSP00000507499.1:n.303+158T>G
|
|
ENST00000682303.1:c.*2861T>G
|
ENSP00000508325.1:n.*2861T>G
|
|
ENST00000682308.1:c.3075T>G
|
ENSP00000507056.1:p.Ser1025=
|
|
ENST00000682480.1:c.3093T>G
|
ENSP00000508344.1:p.Ser1031=
|
|
ENST00000682546.1:c.3072T>G
|
ENSP00000508188.1:p.Ser1024=
|
|
ENST00000682585.1:c.3075T>G
|
ENSP00000506885.1:p.Ser1025=
|
|
ENST00000682595.1:n.3659T>G
|
|
|
ENST00000682607.1:c.1493T>G
|
|
|
ENST00000682779.1:c.3066T>G
|
ENSP00000507947.1:p.Ser1022=
|
|
ENST00000682845.1:n.2177T>G
|
|
|
ENST00000682885.1:c.3030T>G
|
ENSP00000508036.1:p.Ser1010=
|
|
ENST00000682933.1:n.3149T>G
|
|
|
ENST00000683072.1:n.3659T>G
|
|
|
ENST00000683080.1:n.694T>G
|
|
|
ENST00000683125.1:c.3183T>G
|
ENSP00000507939.1:p.Ser1061=
|
|
ENST00000683213.1:c.3078T>G
|
ENSP00000507751.1:p.Ser1026=
|
|
ENST00000683220.1:c.3105T>G
|
ENSP00000507151.1:p.Ser1035=
|
|
ENST00000683329.1:n.3878T>G
|
|
|
ENST00000683346.1:c.*2950T>G
|
ENSP00000507458.1:n.*2950T>G
|
|
ENST00000683409.1:n.1682T>G
|
|
|
ENST00000683459.1:n.3662T>G
|
|
|
ENST00000683590.1:c.2897-5540T>G
|
ENSP00000506820.1:n.2897-5540T>G
|
|
ENST00000683623.1:c.2982T>G
|
ENSP00000507702.1:p.Ser994=
|
|
ENST00000683645.1:n.3626T>G
|
|
|
ENST00000683796.1:c.*2947T>G
|
ENSP00000508221.1:n.*2947T>G
|
|
ENST00000683802.1:n.6000T>G
|
|
|
ENST00000683833.1:c.3066T>G
|
ENSP00000506852.1:p.Ser1022=
|
|
ENST00000683994.1:c.3075T>G
|
ENSP00000507181.1:p.Ser1025=
|
|
ENST00000684290.1:c.*611T>G
|
ENSP00000507243.1:n.*611T>G
|
|
ENST00000684306.1:c.*2988T>G
|
ENSP00000508384.1:n.*2988T>G
|
|
ENST00000684341.1:n.3095T>G
|
|
|
ENST00000684383.1:c.*2713T>G
|
ENSP00000506863.1:n.*2713T>G
|
|
ENST00000684619.1:c.*2947T>G
|
ENSP00000508088.1:n.*2947T>G
|
|
ENST00000684705.1:n.196T>G
|
|
|
ENST00000684743.1:n.4106T>G
|
|
|
ENST00000260665.12:c.3075T>G
MANE Select
|
ENSP00000260665.7:p.Ser1025=
|
|
ENST00000260665.11:c.3075T>G
|
ENSP00000260665.7:p.Ser1025=
|
|
NM_133259.3:c.3075T>G
|
NP_573566.2:p.Ser1025=
|
|
XM_006711915.2:c.2997T>G
|
XP_006711978.1:p.Ser999=
|
|
XM_006711916.2:c.3075T>G
|
XP_006711979.1:p.Ser1025=
|
|
XM_011532473.1:c.3075T>G
|
XP_011530775.1:p.Ser1025=
|
|
XM_011532474.1:c.3075T>G
|
XP_011530776.1:p.Ser1025=
|
|
XM_006711916.3:c.3075T>G
|
XP_006711979.1:p.Ser1025=
|
|
XM_017003117.1:c.2997T>G
|
XP_016858606.1:p.Ser999=
|
|
XR_002958896.1:n.3117T>G
|
|
|
NM_133259.4:c.3075T>G
MANE Select
|
NP_573566.2:p.Ser1025=
|
|