|
ENST00000419884.6:c.216T>A
|
|
|
|
ENST00000472420.6:n.864T>A
|
|
|
|
ENST00000483489.2:n.216T>A
|
|
|
|
ENST00000681993.1:n.1337T>A
|
|
|
|
ENST00000682303.1:c.*3571T>A
|
ENSP00000508325.1:n.*3571T>A
|
|
|
ENST00000682308.1:c.3785T>A
|
ENSP00000507056.1:p.Val1262Glu
|
|
|
ENST00000682434.1:n.1336T>A
|
|
|
|
ENST00000682480.1:c.3803T>A
|
ENSP00000508344.1:p.Val1268Glu
|
|
|
ENST00000682546.1:c.3782T>A
|
ENSP00000508188.1:p.Val1261Glu
|
|
|
ENST00000682585.1:c.3785T>A
|
ENSP00000506885.1:p.Val1262Glu
|
|
|
ENST00000682595.1:n.4369T>A
|
|
|
|
ENST00000682607.1:c.2203T>A
|
|
|
|
ENST00000682612.1:c.637T>A
|
|
|
|
ENST00000682779.1:c.3776T>A
|
ENSP00000507947.1:p.Val1259Glu
|
|
|
ENST00000682845.1:n.2887T>A
|
|
|
|
ENST00000682885.1:c.3740T>A
|
ENSP00000508036.1:p.Val1247Glu
|
|
|
ENST00000682933.1:n.3859T>A
|
|
|
|
ENST00000683002.1:c.637T>A
|
|
|
|
ENST00000683072.1:n.4369T>A
|
|
|
|
ENST00000683080.1:n.1404T>A
|
|
|
|
ENST00000683125.1:c.3893T>A
|
ENSP00000507939.1:p.Val1298Glu
|
|
|
ENST00000683213.1:c.3788T>A
|
ENSP00000507751.1:p.Val1263Glu
|
|
|
ENST00000683220.1:c.3815T>A
|
ENSP00000507151.1:p.Val1272Glu
|
|
|
ENST00000683329.1:n.4588T>A
|
|
|
|
ENST00000683346.1:c.*3660T>A
|
ENSP00000507458.1:n.*3660T>A
|
|
|
ENST00000683409.1:n.2392T>A
|
|
|
|
ENST00000683459.1:n.4372T>A
|
|
|
|
ENST00000683528.1:c.713T>A
|
|
|
|
ENST00000683590.1:c.3533T>A
|
ENSP00000506820.1:p.Val1178Glu
|
|
|
ENST00000683623.1:c.3692T>A
|
ENSP00000507702.1:p.Val1231Glu
|
|
|
ENST00000683645.1:n.4336T>A
|
|
|
|
ENST00000683796.1:c.*3657T>A
|
ENSP00000508221.1:n.*3657T>A
|
|
|
ENST00000683802.1:n.6710T>A
|
|
|
|
ENST00000683833.1:c.3776T>A
|
ENSP00000506852.1:p.Val1259Glu
|
|
|
ENST00000683994.1:c.3785T>A
|
ENSP00000507181.1:p.Val1262Glu
|
|
|
ENST00000684290.1:c.*1321T>A
|
ENSP00000507243.1:n.*1321T>A
|
|
|
ENST00000684306.1:c.*3698T>A
|
ENSP00000508384.1:n.*3698T>A
|
|
|
ENST00000684341.1:n.3805T>A
|
|
|
|
ENST00000684383.1:c.*3423T>A
|
ENSP00000506863.1:n.*3423T>A
|
|
|
ENST00000684418.1:n.4966T>A
|
|
|
|
ENST00000684433.1:n.169T>A
|
|
|
|
ENST00000684454.1:n.3135T>A
|
|
|
|
ENST00000684619.1:c.*3657T>A
|
ENSP00000508088.1:n.*3657T>A
|
|
|
ENST00000684743.1:n.6530T>A
|
|
|
|
ENST00000260665.12:c.3785T>A
MANE Select
|
ENSP00000260665.7:p.Val1262Glu
|
|
|
ENST00000260665.11:c.3785T>A
|
ENSP00000260665.7:p.Val1262Glu
|
|
|
ENST00000419884.5:c.26T>A
|
ENSP00000414207.1:p.Val9Glu
|
|
|
ENST00000463456.5:n.2828T>A
|
|
|
|
ENST00000472420.5:n.182T>A
|
|
|
|
ENST00000483489.1:n.259T>A
|
|
|
|
NM_133259.3:c.3785T>A
|
NP_573566.2:p.Val1262Glu
|
|
|
XM_006711915.2:c.3707T>A
|
XP_006711978.1:p.Val1236Glu
|
|
|
XM_011532473.1:c.3785T>A
|
XP_011530775.1:p.Val1262Glu
|
|
|
XM_011532474.1:c.3785T>A
|
XP_011530776.1:p.Val1262Glu
|
|
|
XM_017003117.1:c.3707T>A
|
XP_016858606.1:p.Val1236Glu
|
|
|
XR_002958896.1:n.3827T>A
|
|
|
|
NM_133259.4:c.3785T>A
MANE Select
|
NP_573566.2:p.Val1262Glu
|
|
