ENST00000681993.1:n.638C>A
|
|
|
ENST00000682295.1:c.303+169C>A
|
ENSP00000507499.1:n.303+169C>A
|
|
ENST00000682303.1:c.*2872C>A
|
ENSP00000508325.1:n.*2872C>A
|
|
ENST00000682308.1:c.3086C>A
|
ENSP00000507056.1:p.Ser1029Ter
|
|
ENST00000682480.1:c.3104C>A
|
ENSP00000508344.1:p.Ser1035Ter
|
|
ENST00000682546.1:c.3083C>A
|
ENSP00000508188.1:p.Ser1028Ter
|
|
ENST00000682585.1:c.3086C>A
|
ENSP00000506885.1:p.Ser1029Ter
|
|
ENST00000682595.1:n.3670C>A
|
|
|
ENST00000682607.1:c.1504C>A
|
|
|
ENST00000682779.1:c.3077C>A
|
ENSP00000507947.1:p.Ser1026Ter
|
|
ENST00000682845.1:n.2188C>A
|
|
|
ENST00000682885.1:c.3041C>A
|
ENSP00000508036.1:p.Ser1014Ter
|
|
ENST00000682933.1:n.3160C>A
|
|
|
ENST00000683072.1:n.3670C>A
|
|
|
ENST00000683080.1:n.705C>A
|
|
|
ENST00000683125.1:c.3194C>A
|
ENSP00000507939.1:p.Ser1065Ter
|
|
ENST00000683213.1:c.3089C>A
|
ENSP00000507751.1:p.Ser1030Ter
|
|
ENST00000683220.1:c.3116C>A
|
ENSP00000507151.1:p.Ser1039Ter
|
|
ENST00000683329.1:n.3889C>A
|
|
|
ENST00000683346.1:c.*2961C>A
|
ENSP00000507458.1:n.*2961C>A
|
|
ENST00000683409.1:n.1693C>A
|
|
|
ENST00000683459.1:n.3673C>A
|
|
|
ENST00000683590.1:c.2897-5529C>A
|
ENSP00000506820.1:n.2897-5529C>A
|
|
ENST00000683623.1:c.2993C>A
|
ENSP00000507702.1:p.Ser998Ter
|
|
ENST00000683645.1:n.3637C>A
|
|
|
ENST00000683796.1:c.*2958C>A
|
ENSP00000508221.1:n.*2958C>A
|
|
ENST00000683802.1:n.6011C>A
|
|
|
ENST00000683833.1:c.3077C>A
|
ENSP00000506852.1:p.Ser1026Ter
|
|
ENST00000683994.1:c.3086C>A
|
ENSP00000507181.1:p.Ser1029Ter
|
|
ENST00000684290.1:c.*622C>A
|
ENSP00000507243.1:n.*622C>A
|
|
ENST00000684306.1:c.*2999C>A
|
ENSP00000508384.1:n.*2999C>A
|
|
ENST00000684341.1:n.3106C>A
|
|
|
ENST00000684383.1:c.*2724C>A
|
ENSP00000506863.1:n.*2724C>A
|
|
ENST00000684619.1:c.*2958C>A
|
ENSP00000508088.1:n.*2958C>A
|
|
ENST00000684705.1:n.207C>A
|
|
|
ENST00000684743.1:n.4117C>A
|
|
|
ENST00000260665.12:c.3086C>A
MANE Select
|
ENSP00000260665.7:p.Ser1029Ter
|
|
ENST00000260665.11:c.3086C>A
|
ENSP00000260665.7:p.Ser1029Ter
|
|
NM_133259.3:c.3086C>A
|
NP_573566.2:p.Ser1029Ter
|
|
XM_006711915.2:c.3008C>A
|
XP_006711978.1:p.Ser1003Ter
|
|
XM_006711916.2:c.3086C>A
|
XP_006711979.1:p.Ser1029Ter
|
|
XM_011532473.1:c.3086C>A
|
XP_011530775.1:p.Ser1029Ter
|
|
XM_011532474.1:c.3086C>A
|
XP_011530776.1:p.Ser1029Ter
|
|
XM_006711916.3:c.3086C>A
|
XP_006711979.1:p.Ser1029Ter
|
|
XM_017003117.1:c.3008C>A
|
XP_016858606.1:p.Ser1003Ter
|
|
XR_002958896.1:n.3128C>A
|
|
|
NM_133259.4:c.3086C>A
MANE Select
|
NP_573566.2:p.Ser1029Ter
|
|