|
ENST00000370841.9:c.1016G>C
MANE Select
|
ENSP00000359878.5:p.Arg339Thr
|
|
|
ENST00000473018.3:n.3140G>C
|
|
|
|
ENST00000532207.6:n.2027G>C
|
|
|
|
ENST00000541113.6:c.920G>C
|
ENSP00000442324.2:p.Arg307Thr
|
|
|
ENST00000679509.1:n.1978G>C
|
|
|
|
ENST00000679530.1:c.*784G>C
|
ENSP00000506454.1:n.*784G>C
|
|
|
ENST00000679615.1:n.3031G>C
|
|
|
|
ENST00000679687.1:c.578G>C
|
ENSP00000506598.1:p.Arg193Thr
|
|
|
ENST00000679704.1:c.*782G>C
|
ENSP00000505117.1:n.*782G>C
|
|
|
ENST00000679709.1:c.*979G>C
|
ENSP00000506623.1:n.*979G>C
|
|
|
ENST00000679976.1:c.*600G>C
|
ENSP00000505565.1:n.*600G>C
|
|
|
ENST00000680166.1:n.4305G>C
|
|
|
|
ENST00000680315.1:n.899G>C
|
|
|
|
ENST00000680517.1:c.*404G>C
|
ENSP00000505803.1:n.*404G>C
|
|
|
ENST00000680582.1:n.1978G>C
|
|
|
|
ENST00000680613.1:c.*509G>C
|
ENSP00000506114.1:n.*509G>C
|
|
|
ENST00000680662.1:c.*930G>C
|
ENSP00000505080.1:n.*930G>C
|
|
|
ENST00000680691.1:c.*679G>C
|
ENSP00000506487.1:n.*679G>C
|
|
|
ENST00000680694.1:c.*604G>C
|
ENSP00000505658.1:n.*604G>C
|
|
|
ENST00000680743.1:c.*805G>C
|
ENSP00000505073.1:n.*805G>C
|
|
|
ENST00000680749.1:c.*301G>C
|
ENSP00000505122.1:n.*301G>C
|
|
|
ENST00000680798.1:c.*491G>C
|
ENSP00000505670.1:n.*491G>C
|
|
|
ENST00000680805.1:c.875G>C
|
ENSP00000505447.1:p.Arg292Thr
|
|
|
ENST00000680844.1:c.*800G>C
|
ENSP00000506541.1:n.*800G>C
|
|
|
ENST00000680948.1:c.*883G>C
|
ENSP00000505441.1:n.*883G>C
|
|
|
ENST00000680964.1:c.*109G>C
|
ENSP00000505961.1:n.*109G>C
|
|
|
ENST00000681037.1:c.*2500G>C
|
ENSP00000506025.1:n.*2500G>C
|
|
|
ENST00000681063.1:c.*285G>C
|
ENSP00000506616.1:n.*285G>C
|
|
|
ENST00000681209.1:c.*671G>C
|
ENSP00000505877.1:n.*671G>C
|
|
|
ENST00000681278.1:n.1718G>C
|
|
|
|
ENST00000681289.1:n.5011G>C
|
|
|
|
ENST00000681361.1:c.*683G>C
|
ENSP00000506679.1:n.*683G>C
|
|
|
ENST00000681430.1:c.*109G>C
|
ENSP00000506301.1:n.*109G>C
|
|
|
ENST00000681446.1:c.*720G>C
|
ENSP00000506244.1:n.*720G>C
|
|
|
ENST00000681450.1:c.*687G>C
|
ENSP00000505660.1:n.*687G>C
|
|
|
ENST00000681548.1:c.*602G>C
|
ENSP00000505275.1:n.*602G>C
|
|
|
ENST00000681616.1:c.*675G>C
|
ENSP00000505111.1:n.*675G>C
|
|
|
ENST00000681621.1:c.*600G>C
|
ENSP00000505770.1:n.*600G>C
|
|
|
ENST00000681680.1:n.3111G>C
|
|
|
|
ENST00000681720.1:c.*471G>C
|
ENSP00000505438.1:n.*471G>C
|
|
|
ENST00000681730.1:n.1238G>C
|
|
|
|
ENST00000681790.1:c.758G>C
|
ENSP00000505130.1:p.Arg253Thr
|
|
|
ENST00000681837.1:n.1632G>C
|
|
|
|
ENST00000681913.1:n.3262G>C
|
|
|
|
ENST00000681916.1:c.*784G>C
|
ENSP00000506477.1:n.*784G>C
|
|
|
ENST00000681930.1:n.3140G>C
|
|
|
|
ENST00000370834.9:c.1115G>C
|
ENSP00000359871.5:p.Arg372Thr
|
|
|
ENST00000370841.8:c.1016G>C
|
ENSP00000359878.4:p.Arg339Thr
|
|
|
ENST00000420607.6:c.1028G>C
|
ENSP00000409612.2:p.Arg343Thr
|
|
|
ENST00000481374.1:n.289G>C
|
|
|
|
ENST00000525808.5:c.*602G>C
|
ENSP00000434823.1:n.*602G>C
|
|
|
ENST00000526129.5:c.*800G>C
|
ENSP00000434092.1:n.*800G>C
|
|
|
ENST00000526196.5:c.*784G>C
|
ENSP00000431953.1:n.*784G>C
|
|
|
ENST00000528016.1:c.160-7985G>C
|
ENSP00000434284.1:n.160-7985G>C
|
|
|
ENST00000529059.5:n.925G>C
|
|
|
|
ENST00000532207.5:n.746G>C
|
|
|
|
ENST00000534334.5:c.*757G>C
|
ENSP00000435584.1:n.*757G>C
|
|
|
ENST00000541113.5:c.908G>C
|
ENSP00000442324.1:p.Arg303Thr
|
|
|
NM_000016.5:c.1016G>C
|
NP_000007.1:p.Arg339Thr
|
|
|
NM_001127328.2:c.1028G>C
|
NP_001120800.1:p.Arg343Thr
|
|
|
NM_001286042.1:c.908G>C
|
NP_001272971.1:p.Arg303Thr
|
|
|
NM_001286043.1:c.1115G>C
|
NP_001272972.1:p.Arg372Thr
|
|
|
NM_001286044.1:c.449G>C
|
NP_001272973.1:p.Arg150Thr
|
|
|
NM_000016.6:c.1016G>C
MANE Select
|
NP_000007.1:p.Arg339Thr
|
|
|
NM_001127328.3:c.1028G>C
|
NP_001120800.1:p.Arg343Thr
|
|
|
NM_001286042.2:c.908G>C
|
NP_001272971.1:p.Arg303Thr
|
|
|
NM_001286043.2:c.1115G>C
|
NP_001272972.1:p.Arg372Thr
|
|
|
NM_001286044.2:c.449G>C
|
NP_001272973.1:p.Arg150Thr
|
|
