ENST00000472420.6:n.389G=
|
|
|
ENST00000681993.1:n.862G=
|
|
|
ENST00000682295.1:c.465G=
|
ENSP00000507499.1:n.465G=
|
|
ENST00000682303.1:c.*3096G=
|
ENSP00000508325.1:n.*3096G=
|
|
ENST00000682308.1:c.3310G=
|
ENSP00000507056.1:p.Asp1104=
|
|
ENST00000682480.1:c.3328G=
|
ENSP00000508344.1:p.Asp1110=
|
|
ENST00000682546.1:c.3307G=
|
ENSP00000508188.1:p.Asp1103=
|
|
ENST00000682585.1:c.3310G=
|
ENSP00000506885.1:p.Asp1104=
|
|
ENST00000682595.1:n.3894G=
|
|
|
ENST00000682607.1:c.1728G=
|
|
|
ENST00000682612.1:c.162G=
|
|
|
ENST00000682779.1:c.3301G=
|
ENSP00000507947.1:p.Asp1101=
|
|
ENST00000682845.1:n.2412G=
|
|
|
ENST00000682885.1:c.3265G=
|
ENSP00000508036.1:p.Asp1089=
|
|
ENST00000682933.1:n.3384G=
|
|
|
ENST00000683002.1:c.162G=
|
|
|
ENST00000683072.1:n.3894G=
|
|
|
ENST00000683080.1:n.929G=
|
|
|
ENST00000683125.1:c.3418G=
|
ENSP00000507939.1:p.Asp1140=
|
|
ENST00000683213.1:c.3313G=
|
ENSP00000507751.1:p.Asp1105=
|
|
ENST00000683220.1:c.3340G=
|
ENSP00000507151.1:p.Asp1114=
|
|
ENST00000683329.1:n.4113G=
|
|
|
ENST00000683346.1:c.*3185G=
|
ENSP00000507458.1:n.*3185G=
|
|
ENST00000683409.1:n.1917G=
|
|
|
ENST00000683459.1:n.3897G=
|
|
|
ENST00000683528.1:c.162G=
|
|
|
ENST00000683590.1:c.3058G=
|
ENSP00000506820.1:p.Asp1020=
|
|
ENST00000683623.1:c.3217G=
|
ENSP00000507702.1:p.Asp1073=
|
|
ENST00000683645.1:n.3861G=
|
|
|
ENST00000683796.1:c.*3182G=
|
ENSP00000508221.1:n.*3182G=
|
|
ENST00000683802.1:n.6235G=
|
|
|
ENST00000683833.1:c.3301G=
|
ENSP00000506852.1:p.Asp1101=
|
|
ENST00000683994.1:c.3310G=
|
ENSP00000507181.1:p.Asp1104=
|
|
ENST00000684290.1:c.*846G=
|
ENSP00000507243.1:n.*846G=
|
|
ENST00000684306.1:c.*3223G=
|
ENSP00000508384.1:n.*3223G=
|
|
ENST00000684341.1:n.3330G=
|
|
|
ENST00000684383.1:c.*2948G=
|
ENSP00000506863.1:n.*2948G=
|
|
ENST00000684418.1:n.4491G=
|
|
|
ENST00000684454.1:n.2660G=
|
|
|
ENST00000684619.1:c.*3182G=
|
ENSP00000508088.1:n.*3182G=
|
|
ENST00000684743.1:n.4341G=
|
|
|
ENST00000260665.12:c.3310G=
MANE Select
|
ENSP00000260665.7:p.Asp1104=
|
|
ENST00000260665.11:c.3310G=
|
ENSP00000260665.7:p.Asp1104=
|
|
NM_133259.3:c.3310G=
|
NP_573566.2:p.Asp1104=
|
|
XM_006711915.2:c.3232G=
|
XP_006711978.1:p.Asp1078=
|
|
XM_011532473.1:c.3310G=
|
XP_011530775.1:p.Asp1104=
|
|
XM_011532474.1:c.3310G=
|
XP_011530776.1:p.Asp1104=
|
|
XM_017003117.1:c.3232G=
|
XP_016858606.1:p.Asp1078=
|
|
XR_002958896.1:n.3352G=
|
|
|
NM_133259.4:c.3310G=
MANE Select
|
NP_573566.2:p.Asp1104=
|
|