ENST00000472420.6:n.370C>G
|
|
|
ENST00000681993.1:n.843C>G
|
|
|
ENST00000682295.1:c.446C>G
|
ENSP00000507499.1:n.446C>G
|
|
ENST00000682303.1:c.*3077C>G
|
ENSP00000508325.1:n.*3077C>G
|
|
ENST00000682308.1:c.3291C>G
|
ENSP00000507056.1:p.Ile1097Met
|
|
ENST00000682480.1:c.3309C>G
|
ENSP00000508344.1:p.Ile1103Met
|
|
ENST00000682546.1:c.3288C>G
|
ENSP00000508188.1:p.Ile1096Met
|
|
ENST00000682585.1:c.3291C>G
|
ENSP00000506885.1:p.Ile1097Met
|
|
ENST00000682595.1:n.3875C>G
|
|
|
ENST00000682607.1:c.1709C>G
|
|
|
ENST00000682612.1:c.143C>G
|
|
|
ENST00000682779.1:c.3282C>G
|
ENSP00000507947.1:p.Ile1094Met
|
|
ENST00000682845.1:n.2393C>G
|
|
|
ENST00000682885.1:c.3246C>G
|
ENSP00000508036.1:p.Ile1082Met
|
|
ENST00000682933.1:n.3365C>G
|
|
|
ENST00000683002.1:c.143C>G
|
|
|
ENST00000683072.1:n.3875C>G
|
|
|
ENST00000683080.1:n.910C>G
|
|
|
ENST00000683125.1:c.3399C>G
|
ENSP00000507939.1:p.Ile1133Met
|
|
ENST00000683213.1:c.3294C>G
|
ENSP00000507751.1:p.Ile1098Met
|
|
ENST00000683220.1:c.3321C>G
|
ENSP00000507151.1:p.Ile1107Met
|
|
ENST00000683329.1:n.4094C>G
|
|
|
ENST00000683346.1:c.*3166C>G
|
ENSP00000507458.1:n.*3166C>G
|
|
ENST00000683409.1:n.1898C>G
|
|
|
ENST00000683459.1:n.3878C>G
|
|
|
ENST00000683528.1:c.143C>G
|
|
|
ENST00000683590.1:c.3039C>G
|
ENSP00000506820.1:p.Ile1013Met
|
|
ENST00000683623.1:c.3198C>G
|
ENSP00000507702.1:p.Ile1066Met
|
|
ENST00000683645.1:n.3842C>G
|
|
|
ENST00000683796.1:c.*3163C>G
|
ENSP00000508221.1:n.*3163C>G
|
|
ENST00000683802.1:n.6216C>G
|
|
|
ENST00000683833.1:c.3282C>G
|
ENSP00000506852.1:p.Ile1094Met
|
|
ENST00000683994.1:c.3291C>G
|
ENSP00000507181.1:p.Ile1097Met
|
|
ENST00000684290.1:c.*827C>G
|
ENSP00000507243.1:n.*827C>G
|
|
ENST00000684306.1:c.*3204C>G
|
ENSP00000508384.1:n.*3204C>G
|
|
ENST00000684341.1:n.3311C>G
|
|
|
ENST00000684383.1:c.*2929C>G
|
ENSP00000506863.1:n.*2929C>G
|
|
ENST00000684418.1:n.4472C>G
|
|
|
ENST00000684454.1:n.2641C>G
|
|
|
ENST00000684619.1:c.*3163C>G
|
ENSP00000508088.1:n.*3163C>G
|
|
ENST00000684743.1:n.4322C>G
|
|
|
ENST00000260665.12:c.3291C>G
MANE Select
|
ENSP00000260665.7:p.Ile1097Met
|
|
ENST00000260665.11:c.3291C>G
|
ENSP00000260665.7:p.Ile1097Met
|
|
NM_133259.3:c.3291C>G
|
NP_573566.2:p.Ile1097Met
|
|
XM_006711915.2:c.3213C>G
|
XP_006711978.1:p.Ile1071Met
|
|
XM_011532473.1:c.3291C>G
|
XP_011530775.1:p.Ile1097Met
|
|
XM_011532474.1:c.3291C>G
|
XP_011530776.1:p.Ile1097Met
|
|
XM_017003117.1:c.3213C>G
|
XP_016858606.1:p.Ile1071Met
|
|
XR_002958896.1:n.3333C>G
|
|
|
NM_133259.4:c.3291C>G
MANE Select
|
NP_573566.2:p.Ile1097Met
|
|