|
ENST00000354674.5:c.2240T>C
MANE Plus Clinical
|
ENSP00000346701.4:p.Ile747Thr
|
|
|
ENST00000367255.10:c.25706T>C
MANE Select
|
ENSP00000356224.5:p.Ile8569Thr
|
|
|
ENST00000423061.6:c.25562T>C
|
ENSP00000396024.1:p.Ile8521Thr
|
|
|
ENST00000672154.1:c.1108T>C
|
|
|
|
ENST00000672169.1:c.1483T>C
|
|
|
|
ENST00000673173.1:c.1350T>C
|
|
|
|
ENST00000673451.1:c.1478T>C
|
ENSP00000500189.1:p.Ile493Thr
|
|
|
ENST00000341594.9:c.24491T>C
|
ENSP00000341887.6:p.Ile8164Thr
|
|
|
ENST00000347037.9:n.2454T>C
|
|
|
|
ENST00000354674.4:c.2240T>C
|
ENSP00000346701.4:p.Ile747Thr
|
|
|
ENST00000367251.7:c.4541T>C
|
ENSP00000356220.3:p.Ile1514Thr
|
|
|
ENST00000367255.9:c.25706T>C
|
ENSP00000356224.5:p.Ile8569Thr
|
|
|
ENST00000367256.9:n.9398T>C
|
|
|
|
ENST00000367257.8:c.3644T>C
|
ENSP00000356226.4:p.Ile1215Thr
|
|
|
ENST00000409694.6:n.9290T>C
|
|
|
|
ENST00000423061.5:c.25562T>C
|
ENSP00000396024.1:p.Ile8521Thr
|
|
|
ENST00000460912.6:n.2320T>C
|
|
|
|
ENST00000478916.5:n.4728T>C
|
|
|
|
ENST00000536990.5:n.2543T>C
|
|
|
|
ENST00000539504.5:c.2171T>C
|
ENSP00000441052.1:p.Ile724Thr
|
|
|
NM_033071.3:c.25562T>C
|
NP_149062.1:p.Ile8521Thr
|
|
|
NM_182961.3:c.25706T>C
|
NP_892006.3:p.Ile8569Thr
|
|
|
XM_006715407.1:c.25853T>C
|
XP_006715470.1:p.Ile8618Thr
|
|
|
XM_006715408.1:c.25841T>C
|
XP_006715471.1:p.Ile8614Thr
|
|
|
XM_006715409.1:c.25832T>C
|
XP_006715472.1:p.Ile8611Thr
|
|
|
XM_006715410.1:c.25811T>C
|
XP_006715473.1:p.Ile8604Thr
|
|
|
XM_006715411.1:c.25802T>C
|
XP_006715474.1:p.Ile8601Thr
|
|
|
XM_006715412.1:c.25796T>C
|
XP_006715475.1:p.Ile8599Thr
|
|
|
XM_006715413.1:c.25784T>C
|
XP_006715476.1:p.Ile8595Thr
|
|
|
XM_006715414.1:c.25781T>C
|
XP_006715477.1:p.Ile8594Thr
|
|
|
XM_006715415.1:c.25742T>C
|
XP_006715478.1:p.Ile8581Thr
|
|
|
XM_006715416.1:c.25727T>C
|
XP_006715479.1:p.Ile8576Thr
|
|
|
XM_006715417.1:c.25712T>C
|
XP_006715480.1:p.Ile8571Thr
|
|
|
XM_006715420.1:c.25700T>C
|
XP_006715483.1:p.Ile8567Thr
|
|
|
XM_006715421.1:c.25697T>C
|
XP_006715484.1:p.Ile8566Thr
|
|
|
XM_006715422.1:c.25694T>C
|
XP_006715485.1:p.Ile8565Thr
|
|
|
XM_006715423.1:c.25853T>C
|
XP_006715486.1:p.Ile8618Thr
|
|
|
XM_006715424.1:c.25811T>C
|
XP_006715487.1:p.Ile8604Thr
|
|
|
XM_006715425.1:c.25742T>C
|
XP_006715488.1:p.Ile8581Thr
|
|
|
XM_011535641.1:c.25850T>C
|
XP_011533943.1:p.Ile8617Thr
|
|
|
XM_011535642.1:c.25838T>C
|
XP_011533944.1:p.Ile8613Thr
|
|
|
XM_011535643.1:c.25688T>C
|
XP_011533945.1:p.Ile8563Thr
|
|
|
XM_011535644.1:c.24128T>C
|
XP_011533946.1:p.Ile8043Thr
|
|
|
XM_011535645.1:c.23621T>C
|
XP_011533947.1:p.Ile7874Thr
|
|
|
XM_011535647.1:c.19088T>C
|
XP_011533949.1:p.Ile6363Thr
|
|
|
NM_001347701.1:c.2312T>C
|
NP_001334630.1:p.Ile771Thr
|
|
|
NM_001347702.1:c.2240T>C
|
NP_001334631.1:p.Ile747Thr
|
|
|
XM_006715408.2:c.25841T>C
|
XP_006715471.1:p.Ile8614Thr
|
|
|
XM_006715410.2:c.25811T>C
|
XP_006715473.1:p.Ile8604Thr
|
|
|
XM_006715412.2:c.25796T>C
|
XP_006715475.1:p.Ile8599Thr
|
|
|
XM_006715413.2:c.25784T>C
|
XP_006715476.1:p.Ile8595Thr
|
|
|
XM_006715415.2:c.25742T>C
|
XP_006715478.1:p.Ile8581Thr
|
|
|
XM_006715416.2:c.25727T>C
|
XP_006715479.1:p.Ile8576Thr
|
|
|
XM_006715417.2:c.25712T>C
|
XP_006715480.1:p.Ile8571Thr
|
|
|
XM_006715420.2:c.25700T>C
|
XP_006715483.1:p.Ile8567Thr
|
|
|
XM_006715421.2:c.25697T>C
|
XP_006715484.1:p.Ile8566Thr
|
|
|
XM_006715423.2:c.25853T>C
|
XP_006715486.1:p.Ile8618Thr
|
|
|
XM_006715424.2:c.25811T>C
|
XP_006715487.1:p.Ile8604Thr
|
|
|
XM_006715425.2:c.25742T>C
|
XP_006715488.1:p.Ile8581Thr
|
|
|
XM_011535641.2:c.25850T>C
|
XP_011533943.1:p.Ile8617Thr
|
|
|
XM_011535642.2:c.25838T>C
|
XP_011533944.1:p.Ile8613Thr
|
|
|
XM_011535645.2:c.23621T>C
|
XP_011533947.1:p.Ile7874Thr
|
|
|
XM_017010608.1:c.25853T>C
|
XP_016866097.1:p.Ile8618Thr
|
|
|
XM_017010609.1:c.25853T>C
|
XP_016866098.1:p.Ile8618Thr
|
|
|
XM_017010610.1:c.25832T>C
|
XP_016866099.1:p.Ile8611Thr
|
|
|
XM_017010611.2:c.25826T>C
|
XP_016866100.1:p.Ile8609Thr
|
|
|
XM_017010612.1:c.25775T>C
|
XP_016866101.1:p.Ile8592Thr
|
|
|
XM_017010613.1:c.25739T>C
|
XP_016866102.1:p.Ile8580Thr
|
|
|
XM_017010614.1:c.25697T>C
|
XP_016866103.1:p.Ile8566Thr
|
|
|
XM_017010615.1:c.25586T>C
|
XP_016866104.1:p.Ile8529Thr
|
|
|
XM_017010616.1:c.25784T>C
|
XP_016866105.1:p.Ile8595Thr
|
|
|
XM_017010617.1:c.25739T>C
|
XP_016866106.1:p.Ile8580Thr
|
|
|
XM_017010618.1:c.25727T>C
|
XP_016866107.1:p.Ile8576Thr
|
|
|
XM_017010619.1:c.24128T>C
|
XP_016866108.1:p.Ile8043Thr
|
|
|
NM_182961.4:c.25706T>C
MANE Select
|
NP_892006.3:p.Ile8569Thr
|
|
|
NM_001347701.2:c.2312T>C
|
NP_001334630.1:p.Ile771Thr
|
|
|
NM_001347702.2:c.2240T>C
MANE Plus Clinical
|
NP_001334631.1:p.Ile747Thr
|
|
|
NM_033071.5:c.25562T>C
|
NP_149062.2:p.Ile8521Thr
|
|
