ENST00000681993.1:n.668T=
|
|
|
ENST00000682295.1:c.303+199T=
|
ENSP00000507499.1:n.303+199T=
|
|
ENST00000682303.1:c.*2902T=
|
ENSP00000508325.1:n.*2902T=
|
|
ENST00000682308.1:c.3116T=
|
ENSP00000507056.1:p.Ile1039=
|
|
ENST00000682480.1:c.3134T=
|
ENSP00000508344.1:p.Ile1045=
|
|
ENST00000682546.1:c.3113T=
|
ENSP00000508188.1:p.Ile1038=
|
|
ENST00000682585.1:c.3116T=
|
ENSP00000506885.1:p.Ile1039=
|
|
ENST00000682595.1:n.3700T=
|
|
|
ENST00000682607.1:c.1534T=
|
|
|
ENST00000682779.1:c.3107T=
|
ENSP00000507947.1:p.Ile1036=
|
|
ENST00000682845.1:n.2218T=
|
|
|
ENST00000682885.1:c.3071T=
|
ENSP00000508036.1:p.Ile1024=
|
|
ENST00000682933.1:n.3190T=
|
|
|
ENST00000683072.1:n.3700T=
|
|
|
ENST00000683080.1:n.735T=
|
|
|
ENST00000683125.1:c.3224T=
|
ENSP00000507939.1:p.Ile1075=
|
|
ENST00000683213.1:c.3119T=
|
ENSP00000507751.1:p.Ile1040=
|
|
ENST00000683220.1:c.3146T=
|
ENSP00000507151.1:p.Ile1049=
|
|
ENST00000683329.1:n.3919T=
|
|
|
ENST00000683346.1:c.*2991T=
|
ENSP00000507458.1:n.*2991T=
|
|
ENST00000683409.1:n.1723T=
|
|
|
ENST00000683459.1:n.3703T=
|
|
|
ENST00000683590.1:c.2897-5499T=
|
ENSP00000506820.1:n.2897-5499T=
|
|
ENST00000683623.1:c.3023T=
|
ENSP00000507702.1:p.Ile1008=
|
|
ENST00000683645.1:n.3667T=
|
|
|
ENST00000683796.1:c.*2988T=
|
ENSP00000508221.1:n.*2988T=
|
|
ENST00000683802.1:n.6041T=
|
|
|
ENST00000683833.1:c.3107T=
|
ENSP00000506852.1:p.Ile1036=
|
|
ENST00000683994.1:c.3116T=
|
ENSP00000507181.1:p.Ile1039=
|
|
ENST00000684290.1:c.*652T=
|
ENSP00000507243.1:n.*652T=
|
|
ENST00000684306.1:c.*3029T=
|
ENSP00000508384.1:n.*3029T=
|
|
ENST00000684341.1:n.3136T=
|
|
|
ENST00000684383.1:c.*2754T=
|
ENSP00000506863.1:n.*2754T=
|
|
ENST00000684619.1:c.*2988T=
|
ENSP00000508088.1:n.*2988T=
|
|
ENST00000684705.1:n.237T=
|
|
|
ENST00000684743.1:n.4147T=
|
|
|
ENST00000260665.12:c.3116T=
MANE Select
|
ENSP00000260665.7:p.Ile1039=
|
|
ENST00000260665.11:c.3116T=
|
ENSP00000260665.7:p.Ile1039=
|
|
NM_133259.3:c.3116T=
|
NP_573566.2:p.Ile1039=
|
|
XM_006711915.2:c.3038T=
|
XP_006711978.1:p.Ile1013=
|
|
XM_006711916.2:c.3116T=
|
XP_006711979.1:p.Ile1039=
|
|
XM_011532473.1:c.3116T=
|
XP_011530775.1:p.Ile1039=
|
|
XM_011532474.1:c.3116T=
|
XP_011530776.1:p.Ile1039=
|
|
XM_006711916.3:c.3116T=
|
XP_006711979.1:p.Ile1039=
|
|
XM_017003117.1:c.3038T=
|
XP_016858606.1:p.Ile1013=
|
|
XR_002958896.1:n.3158T=
|
|
|
NM_133259.4:c.3116T=
MANE Select
|
NP_573566.2:p.Ile1039=
|
|