ENST00000698234.1:n.1486C>A
|
|
|
ENST00000698317.1:n.2102C>A
|
|
|
ENST00000698318.1:n.1885C>A
|
|
|
ENST00000698319.1:n.1248C>A
|
|
|
ENST00000698320.1:n.1136C>A
|
|
|
ENST00000470127.2:n.1149C>A
|
|
|
ENST00000475699.6:c.640C>A
|
ENSP00000419854.3:p.Pro214Thr
|
|
ENST00000483674.3:n.558C>A
|
|
|
ENST00000601016.6:c.676C>A
MANE Select
|
ENSP00000469981.1:p.Pro226Thr
|
|
ENST00000612012.5:c.634C>A
|
ENSP00000482070.2:p.Pro212Thr
|
|
ENST00000612460.5:c.586C>A
|
ENSP00000481037.1:p.Pro196Thr
|
|
ENST00000614595.2:n.2023C>A
|
|
|
ENST00000615658.5:n.1265C>A
|
|
|
ENST00000616020.5:c.688C>A
|
ENSP00000483636.2:p.Pro230Thr
|
|
ENST00000617701.5:c.*689C>A
|
ENSP00000481645.1:n.*689C>A
|
|
ENST00000652354.1:c.358C>A
|
ENSP00000498734.1:p.Pro120Thr
|
|
ENST00000652358.1:c.469C>A
|
ENSP00000498464.1:p.Pro157Thr
|
|
ENST00000652390.1:c.595C>A
|
ENSP00000498858.1:p.Pro199Thr
|
|
ENST00000652476.1:n.1342C>A
|
|
|
ENST00000652644.1:c.289C>A
|
ENSP00000498496.1:p.Pro97Thr
|
|
ENST00000652682.1:c.733C>A
|
ENSP00000498288.1:p.Pro245Thr
|
|
ENST00000652685.1:n.1029C>A
|
|
|
ENST00000369776.8:c.586C>A
|
ENSP00000358791.4:p.Pro196Thr
|
|
ENST00000426231.5:c.673C>A
|
|
|
ENST00000475699.5:c.634C>A
|
ENSP00000419854.2:p.Pro212Thr
|
|
ENST00000494912.5:n.1365C>A
|
|
|
ENST00000498029.1:n.134C>A
|
|
|
ENST00000601016.5:c.676C>A
|
ENSP00000469981.1:p.Pro226Thr
|
|
ENST00000612460.4:c.586C>A
|
ENSP00000481037.1:p.Pro196Thr
|
|
ENST00000613002.4:c.544C>A
|
ENSP00000478154.1:p.Pro182Thr
|
|
ENST00000615986.4:c.*404C>A
|
ENSP00000480133.1:n.*404C>A
|
|
NM_000116.4:c.676C>A
|
NP_000107.1:p.Pro226Thr
|
|
NM_001303465.1:c.688C>A
|
NP_001290394.1:p.Pro230Thr
|
|
NM_181311.3:c.586C>A
|
NP_851828.1:p.Pro196Thr
|
|
NM_181312.3:c.634C>A
|
NP_851829.1:p.Pro212Thr
|
|
NM_181313.3:c.544C>A
|
NP_851830.1:p.Pro182Thr
|
|
NR_024048.2:n.1018C>A
|
|
|
XM_006724836.1:c.730C>A
|
XP_006724899.1:p.Pro244Thr
|
|
XM_006724837.1:c.715C>A
|
XP_006724900.1:p.Pro239Thr
|
|
XM_006724839.1:c.598C>A
|
XP_006724902.1:p.Pro200Thr
|
|
XM_006724841.2:c.469C>A
|
XP_006724904.1:p.Pro157Thr
|
|
XM_006724842.2:c.379C>A
|
XP_006724905.1:p.Pro127Thr
|
|
XM_011531189.1:c.517C>A
|
XP_011529491.1:p.Pro173Thr
|
|
XM_011531190.1:c.469C>A
|
XP_011529492.1:p.Pro157Thr
|
|
XM_011531191.1:c.400C>A
|
XP_011529493.1:p.Pro134Thr
|
|
XM_011531192.1:c.397C>A
|
XP_011529494.1:p.Pro133Thr
|
|
XR_938511.1:n.1024C>A
|
|
|
XM_006724841.4:c.469C>A
|
XP_006724904.1:p.Pro157Thr
|
|
XM_006724842.4:c.379C>A
|
XP_006724905.1:p.Pro127Thr
|
|
XM_011531191.2:c.400C>A
|
XP_011529493.1:p.Pro134Thr
|
|
XM_017029761.1:c.661C>A
|
XP_016885250.1:p.Pro221Thr
|
|
XM_017029762.1:c.640C>A
|
XP_016885251.1:p.Pro214Thr
|
|
XM_017029763.1:c.463C>A
|
XP_016885252.1:p.Pro155Thr
|
|
XM_017029764.1:c.397C>A
|
XP_016885253.1:p.Pro133Thr
|
|
XM_017029765.2:c.337C>A
|
XP_016885254.1:p.Pro113Thr
|
|
XM_024452431.1:c.634C>A
|
XP_024308199.1:p.Pro212Thr
|
|
NM_000116.5:c.676C>A
MANE Select
|
NP_000107.1:p.Pro226Thr
|
|
NM_001303465.2:c.688C>A
|
NP_001290394.1:p.Pro230Thr
|
|
NM_181311.4:c.586C>A
|
NP_851828.1:p.Pro196Thr
|
|
NM_181312.4:c.634C>A
|
NP_851829.1:p.Pro212Thr
|
|
NM_181313.4:c.544C>A
|
NP_851830.1:p.Pro182Thr
|
|
NR_024048.3:n.997C>A
|
|
|