ENST00000472420.6:n.434T>A
|
|
|
ENST00000681993.1:n.907T>A
|
|
|
ENST00000682295.1:c.510T>A
|
ENSP00000507499.1:n.510T>A
|
|
ENST00000682303.1:c.*3141T>A
|
ENSP00000508325.1:n.*3141T>A
|
|
ENST00000682308.1:c.3355T>A
|
ENSP00000507056.1:p.Tyr1119Asn
|
|
ENST00000682480.1:c.3373T>A
|
ENSP00000508344.1:p.Tyr1125Asn
|
|
ENST00000682546.1:c.3352T>A
|
ENSP00000508188.1:p.Tyr1118Asn
|
|
ENST00000682585.1:c.3355T>A
|
ENSP00000506885.1:p.Tyr1119Asn
|
|
ENST00000682595.1:n.3939T>A
|
|
|
ENST00000682607.1:c.1773T>A
|
|
|
ENST00000682612.1:c.207T>A
|
|
|
ENST00000682779.1:c.3346T>A
|
ENSP00000507947.1:p.Tyr1116Asn
|
|
ENST00000682845.1:n.2457T>A
|
|
|
ENST00000682885.1:c.3310T>A
|
ENSP00000508036.1:p.Tyr1104Asn
|
|
ENST00000682933.1:n.3429T>A
|
|
|
ENST00000683002.1:c.207T>A
|
|
|
ENST00000683072.1:n.3939T>A
|
|
|
ENST00000683080.1:n.974T>A
|
|
|
ENST00000683125.1:c.3463T>A
|
ENSP00000507939.1:p.Tyr1155Asn
|
|
ENST00000683213.1:c.3358T>A
|
ENSP00000507751.1:p.Tyr1120Asn
|
|
ENST00000683220.1:c.3385T>A
|
ENSP00000507151.1:p.Tyr1129Asn
|
|
ENST00000683329.1:n.4158T>A
|
|
|
ENST00000683346.1:c.*3230T>A
|
ENSP00000507458.1:n.*3230T>A
|
|
ENST00000683409.1:n.1962T>A
|
|
|
ENST00000683459.1:n.3942T>A
|
|
|
ENST00000683528.1:c.207T>A
|
|
|
ENST00000683590.1:c.3103T>A
|
ENSP00000506820.1:p.Tyr1035Asn
|
|
ENST00000683623.1:c.3262T>A
|
ENSP00000507702.1:p.Tyr1088Asn
|
|
ENST00000683645.1:n.3906T>A
|
|
|
ENST00000683796.1:c.*3227T>A
|
ENSP00000508221.1:n.*3227T>A
|
|
ENST00000683802.1:n.6280T>A
|
|
|
ENST00000683833.1:c.3346T>A
|
ENSP00000506852.1:p.Tyr1116Asn
|
|
ENST00000683994.1:c.3355T>A
|
ENSP00000507181.1:p.Tyr1119Asn
|
|
ENST00000684290.1:c.*891T>A
|
ENSP00000507243.1:n.*891T>A
|
|
ENST00000684306.1:c.*3268T>A
|
ENSP00000508384.1:n.*3268T>A
|
|
ENST00000684341.1:n.3375T>A
|
|
|
ENST00000684383.1:c.*2993T>A
|
ENSP00000506863.1:n.*2993T>A
|
|
ENST00000684418.1:n.4536T>A
|
|
|
ENST00000684454.1:n.2705T>A
|
|
|
ENST00000684619.1:c.*3227T>A
|
ENSP00000508088.1:n.*3227T>A
|
|
ENST00000684743.1:n.4386T>A
|
|
|
ENST00000260665.12:c.3355T>A
MANE Select
|
ENSP00000260665.7:p.Tyr1119Asn
|
|
ENST00000260665.11:c.3355T>A
|
ENSP00000260665.7:p.Tyr1119Asn
|
|
NM_133259.3:c.3355T>A
|
NP_573566.2:p.Tyr1119Asn
|
|
XM_006711915.2:c.3277T>A
|
XP_006711978.1:p.Tyr1093Asn
|
|
XM_011532473.1:c.3355T>A
|
XP_011530775.1:p.Tyr1119Asn
|
|
XM_011532474.1:c.3355T>A
|
XP_011530776.1:p.Tyr1119Asn
|
|
XM_017003117.1:c.3277T>A
|
XP_016858606.1:p.Tyr1093Asn
|
|
XR_002958896.1:n.3397T>A
|
|
|
NM_133259.4:c.3355T>A
MANE Select
|
NP_573566.2:p.Tyr1119Asn
|
|