|
ENST00000419884.6:c.614T>G
|
|
|
|
ENST00000681993.1:n.1536T>G
|
|
|
|
ENST00000682154.1:n.1418T>G
|
|
|
|
ENST00000682303.1:c.*3695T>G
|
ENSP00000508325.1:n.*3695T>G
|
|
|
ENST00000682308.1:c.3909T>G
|
ENSP00000507056.1:p.Tyr1303Ter
|
|
|
ENST00000682434.1:n.3539T>G
|
|
|
|
ENST00000682480.1:c.4002T>G
|
ENSP00000508344.1:p.Tyr1334Ter
|
|
|
ENST00000682546.1:c.3981T>G
|
ENSP00000508188.1:p.Tyr1327Ter
|
|
|
ENST00000682585.1:c.*112T>G
|
ENSP00000506885.1:n.*112T>G
|
|
|
ENST00000682607.1:c.2727T>G
|
|
|
|
ENST00000682612.1:c.752+2088T>G
|
|
|
|
ENST00000682696.1:c.84T>G
|
ENSP00000508411.1:p.Tyr28Ter
|
|
|
ENST00000682779.1:c.3975T>G
|
ENSP00000507947.1:p.Tyr1325Ter
|
|
|
ENST00000682885.1:c.3939T>G
|
ENSP00000508036.1:p.Tyr1313Ter
|
|
|
ENST00000682933.1:n.4184T>G
|
|
|
|
ENST00000683002.1:c.836T>G
|
|
|
|
ENST00000683072.1:n.4568T>G
|
|
|
|
ENST00000683080.1:n.1603T>G
|
|
|
|
ENST00000683096.1:n.2425T>G
|
|
|
|
ENST00000683125.1:c.4092T>G
|
ENSP00000507939.1:p.Tyr1364Ter
|
|
|
ENST00000683213.1:c.3987T>G
|
ENSP00000507751.1:p.Tyr1329Ter
|
|
|
ENST00000683220.1:c.4014T>G
|
ENSP00000507151.1:p.Tyr1338Ter
|
|
|
ENST00000683329.1:n.4787T>G
|
|
|
|
ENST00000683346.1:c.*3859T>G
|
ENSP00000507458.1:n.*3859T>G
|
|
|
ENST00000683409.1:n.2516T>G
|
|
|
|
ENST00000683459.1:n.4571T>G
|
|
|
|
ENST00000683590.1:c.3657T>G
|
ENSP00000506820.1:p.Tyr1219Ter
|
|
|
ENST00000683623.1:c.3891T>G
|
ENSP00000507702.1:p.Tyr1297Ter
|
|
|
ENST00000683796.1:c.*3781T>G
|
ENSP00000508221.1:n.*3781T>G
|
|
|
ENST00000683833.1:c.3900T>G
|
ENSP00000506852.1:p.Tyr1300Ter
|
|
|
ENST00000683994.1:c.*97T>G
|
ENSP00000507181.1:n.*97T>G
|
|
|
ENST00000684290.1:c.*1445T>G
|
ENSP00000507243.1:n.*1445T>G
|
|
|
ENST00000684306.1:c.*3897T>G
|
ENSP00000508384.1:n.*3897T>G
|
|
|
ENST00000684383.1:c.*3622T>G
|
ENSP00000506863.1:n.*3622T>G
|
|
|
ENST00000684418.1:n.5165T>G
|
|
|
|
ENST00000684433.1:n.368T>G
|
|
|
|
ENST00000684454.1:n.7848T>G
|
|
|
|
ENST00000684619.1:c.*3856T>G
|
ENSP00000508088.1:n.*3856T>G
|
|
|
ENST00000684743.1:n.6729T>G
|
|
|
|
ENST00000260665.12:c.3984T>G
MANE Select
|
ENSP00000260665.7:p.Tyr1328Ter
|
|
|
ENST00000260665.11:c.3984T>G
|
ENSP00000260665.7:p.Tyr1328Ter
|
|
|
ENST00000419884.5:c.225T>G
|
ENSP00000414207.1:p.Tyr75Ter
|
|
|
ENST00000463456.5:n.3027T>G
|
|
|
|
NM_133259.3:c.3984T>G
|
NP_573566.2:p.Tyr1328Ter
|
|
|
XM_006711915.2:c.3906T>G
|
XP_006711978.1:p.Tyr1302Ter
|
|
|
XM_011532473.1:c.3909T>G
|
XP_011530775.1:p.Tyr1303Ter
|
|
|
XM_011532474.1:c.3984T>G
|
XP_011530776.1:p.Tyr1328Ter
|
|
|
XM_017003117.1:c.3831T>G
|
XP_016858606.1:p.Tyr1277Ter
|
|
|
XR_002958896.1:n.4026T>G
|
|
|
|
NM_133259.4:c.3984T>G
MANE Select
|
NP_573566.2:p.Tyr1328Ter
|
|
