ENST00000698234.1:n.1483C>A
|
|
|
ENST00000698317.1:n.2099C>A
|
|
|
ENST00000698318.1:n.1882C>A
|
|
|
ENST00000698319.1:n.1245C>A
|
|
|
ENST00000698320.1:n.1133C>A
|
|
|
ENST00000470127.2:n.1146C>A
|
|
|
ENST00000475699.6:c.637C>A
|
ENSP00000419854.3:p.Pro213Thr
|
|
ENST00000483674.3:n.555C>A
|
|
|
ENST00000601016.6:c.673C>A
MANE Select
|
ENSP00000469981.1:p.Pro225Thr
|
|
ENST00000612012.5:c.631C>A
|
ENSP00000482070.2:p.Pro211Thr
|
|
ENST00000612460.5:c.583C>A
|
ENSP00000481037.1:p.Pro195Thr
|
|
ENST00000614595.2:n.2020C>A
|
|
|
ENST00000615658.5:n.1262C>A
|
|
|
ENST00000616020.5:c.685C>A
|
ENSP00000483636.2:p.Pro229Thr
|
|
ENST00000617701.5:c.*686C>A
|
ENSP00000481645.1:n.*686C>A
|
|
ENST00000652354.1:c.355C>A
|
ENSP00000498734.1:p.Pro119Thr
|
|
ENST00000652358.1:c.466C>A
|
ENSP00000498464.1:p.Pro156Thr
|
|
ENST00000652390.1:c.592C>A
|
ENSP00000498858.1:p.Pro198Thr
|
|
ENST00000652476.1:n.1339C>A
|
|
|
ENST00000652644.1:c.286C>A
|
ENSP00000498496.1:p.Pro96Thr
|
|
ENST00000652682.1:c.730C>A
|
ENSP00000498288.1:p.Pro244Thr
|
|
ENST00000652685.1:n.1026C>A
|
|
|
ENST00000369776.8:c.583C>A
|
ENSP00000358791.4:p.Pro195Thr
|
|
ENST00000426231.5:c.670C>A
|
|
|
ENST00000475699.5:c.631C>A
|
ENSP00000419854.2:p.Pro211Thr
|
|
ENST00000494912.5:n.1362C>A
|
|
|
ENST00000498029.1:n.131C>A
|
|
|
ENST00000601016.5:c.673C>A
|
ENSP00000469981.1:p.Pro225Thr
|
|
ENST00000612460.4:c.583C>A
|
ENSP00000481037.1:p.Pro195Thr
|
|
ENST00000613002.4:c.541C>A
|
ENSP00000478154.1:p.Pro181Thr
|
|
ENST00000615986.4:c.*401C>A
|
ENSP00000480133.1:n.*401C>A
|
|
NM_000116.4:c.673C>A
|
NP_000107.1:p.Pro225Thr
|
|
NM_001303465.1:c.685C>A
|
NP_001290394.1:p.Pro229Thr
|
|
NM_181311.3:c.583C>A
|
NP_851828.1:p.Pro195Thr
|
|
NM_181312.3:c.631C>A
|
NP_851829.1:p.Pro211Thr
|
|
NM_181313.3:c.541C>A
|
NP_851830.1:p.Pro181Thr
|
|
NR_024048.2:n.1015C>A
|
|
|
XM_006724836.1:c.727C>A
|
XP_006724899.1:p.Pro243Thr
|
|
XM_006724837.1:c.712C>A
|
XP_006724900.1:p.Pro238Thr
|
|
XM_006724839.1:c.595C>A
|
XP_006724902.1:p.Pro199Thr
|
|
XM_006724841.2:c.466C>A
|
XP_006724904.1:p.Pro156Thr
|
|
XM_006724842.2:c.376C>A
|
XP_006724905.1:p.Pro126Thr
|
|
XM_011531189.1:c.514C>A
|
XP_011529491.1:p.Pro172Thr
|
|
XM_011531190.1:c.466C>A
|
XP_011529492.1:p.Pro156Thr
|
|
XM_011531191.1:c.397C>A
|
XP_011529493.1:p.Pro133Thr
|
|
XM_011531192.1:c.394C>A
|
XP_011529494.1:p.Pro132Thr
|
|
XR_938511.1:n.1021C>A
|
|
|
XM_006724841.4:c.466C>A
|
XP_006724904.1:p.Pro156Thr
|
|
XM_006724842.4:c.376C>A
|
XP_006724905.1:p.Pro126Thr
|
|
XM_011531191.2:c.397C>A
|
XP_011529493.1:p.Pro133Thr
|
|
XM_017029761.1:c.658C>A
|
XP_016885250.1:p.Pro220Thr
|
|
XM_017029762.1:c.637C>A
|
XP_016885251.1:p.Pro213Thr
|
|
XM_017029763.1:c.460C>A
|
XP_016885252.1:p.Pro154Thr
|
|
XM_017029764.1:c.394C>A
|
XP_016885253.1:p.Pro132Thr
|
|
XM_017029765.2:c.334C>A
|
XP_016885254.1:p.Pro112Thr
|
|
XM_024452431.1:c.631C>A
|
XP_024308199.1:p.Pro211Thr
|
|
NM_000116.5:c.673C>A
MANE Select
|
NP_000107.1:p.Pro225Thr
|
|
NM_001303465.2:c.685C>A
|
NP_001290394.1:p.Pro229Thr
|
|
NM_181311.4:c.583C>A
|
NP_851828.1:p.Pro195Thr
|
|
NM_181312.4:c.631C>A
|
NP_851829.1:p.Pro211Thr
|
|
NM_181313.4:c.541C>A
|
NP_851830.1:p.Pro181Thr
|
|
NR_024048.3:n.994C>A
|
|
|