ENST00000698234.1:n.1514T>C
|
|
|
ENST00000698317.1:n.2130T>C
|
|
|
ENST00000698318.1:n.1913T>C
|
|
|
ENST00000698319.1:n.1276T>C
|
|
|
ENST00000698320.1:n.1164T>C
|
|
|
ENST00000470127.2:n.1177T>C
|
|
|
ENST00000475699.6:c.668T>C
|
ENSP00000419854.3:p.Ile223Thr
|
|
ENST00000483674.3:n.586T>C
|
|
|
ENST00000601016.6:c.704T>C
MANE Select
|
ENSP00000469981.1:p.Ile235Thr
|
|
ENST00000612012.5:c.662T>C
|
ENSP00000482070.2:p.Ile221Thr
|
|
ENST00000612460.5:c.614T>C
|
ENSP00000481037.1:p.Ile205Thr
|
|
ENST00000614595.2:n.2051T>C
|
|
|
ENST00000615658.5:n.1293T>C
|
|
|
ENST00000616020.5:c.716T>C
|
ENSP00000483636.2:p.Ile239Thr
|
|
ENST00000617701.5:c.*717T>C
|
ENSP00000481645.1:n.*717T>C
|
|
ENST00000651139.1:c.-80T>C
|
ENSP00000498957.1:n.-80T>C
|
|
ENST00000652354.1:c.386T>C
|
ENSP00000498734.1:p.Ile129Thr
|
|
ENST00000652358.1:c.497T>C
|
ENSP00000498464.1:p.Ile166Thr
|
|
ENST00000652390.1:c.623T>C
|
ENSP00000498858.1:p.Ile208Thr
|
|
ENST00000652476.1:n.1370T>C
|
|
|
ENST00000652644.1:c.317T>C
|
ENSP00000498496.1:p.Ile106Thr
|
|
ENST00000652682.1:c.761T>C
|
ENSP00000498288.1:p.Ile254Thr
|
|
ENST00000652685.1:n.1057T>C
|
|
|
ENST00000369776.8:c.614T>C
|
ENSP00000358791.4:p.Ile205Thr
|
|
ENST00000426231.5:c.701T>C
|
|
|
ENST00000475699.5:c.662T>C
|
ENSP00000419854.2:p.Ile221Thr
|
|
ENST00000494912.5:n.1393T>C
|
|
|
ENST00000498029.1:n.162T>C
|
|
|
ENST00000601016.5:c.704T>C
|
ENSP00000469981.1:p.Ile235Thr
|
|
ENST00000612460.4:c.614T>C
|
ENSP00000481037.1:p.Ile205Thr
|
|
ENST00000613002.4:c.572T>C
|
ENSP00000478154.1:p.Ile191Thr
|
|
ENST00000615986.4:c.*432T>C
|
ENSP00000480133.1:n.*432T>C
|
|
NM_000116.4:c.704T>C
|
NP_000107.1:p.Ile235Thr
|
|
NM_001303465.1:c.716T>C
|
NP_001290394.1:p.Ile239Thr
|
|
NM_181311.3:c.614T>C
|
NP_851828.1:p.Ile205Thr
|
|
NM_181312.3:c.662T>C
|
NP_851829.1:p.Ile221Thr
|
|
NM_181313.3:c.572T>C
|
NP_851830.1:p.Ile191Thr
|
|
NR_024048.2:n.1046T>C
|
|
|
XM_006724836.1:c.758T>C
|
XP_006724899.1:p.Ile253Thr
|
|
XM_006724837.1:c.743T>C
|
XP_006724900.1:p.Ile248Thr
|
|
XM_006724839.1:c.626T>C
|
XP_006724902.1:p.Ile209Thr
|
|
XM_006724841.2:c.497T>C
|
XP_006724904.1:p.Ile166Thr
|
|
XM_006724842.2:c.407T>C
|
XP_006724905.1:p.Ile136Thr
|
|
XM_011531189.1:c.545T>C
|
XP_011529491.1:p.Ile182Thr
|
|
XM_011531190.1:c.497T>C
|
XP_011529492.1:p.Ile166Thr
|
|
XM_011531191.1:c.428T>C
|
XP_011529493.1:p.Ile143Thr
|
|
XM_011531192.1:c.425T>C
|
XP_011529494.1:p.Ile142Thr
|
|
XR_938511.1:n.1052T>C
|
|
|
XM_006724841.4:c.497T>C
|
XP_006724904.1:p.Ile166Thr
|
|
XM_006724842.4:c.407T>C
|
XP_006724905.1:p.Ile136Thr
|
|
XM_011531191.2:c.428T>C
|
XP_011529493.1:p.Ile143Thr
|
|
XM_017029761.1:c.689T>C
|
XP_016885250.1:p.Ile230Thr
|
|
XM_017029762.1:c.668T>C
|
XP_016885251.1:p.Ile223Thr
|
|
XM_017029763.1:c.491T>C
|
XP_016885252.1:p.Ile164Thr
|
|
XM_017029764.1:c.425T>C
|
XP_016885253.1:p.Ile142Thr
|
|
XM_017029765.2:c.365T>C
|
XP_016885254.1:p.Ile122Thr
|
|
XM_024452431.1:c.662T>C
|
XP_024308199.1:p.Ile221Thr
|
|
NM_000116.5:c.704T>C
MANE Select
|
NP_000107.1:p.Ile235Thr
|
|
NM_001303465.2:c.716T>C
|
NP_001290394.1:p.Ile239Thr
|
|
NM_181311.4:c.614T>C
|
NP_851828.1:p.Ile205Thr
|
|
NM_181312.4:c.662T>C
|
NP_851829.1:p.Ile221Thr
|
|
NM_181313.4:c.572T>C
|
NP_851830.1:p.Ile191Thr
|
|
NR_024048.3:n.1025T>C
|
|
|