ENST00000698234.1:n.1551T>G
|
|
|
ENST00000698317.1:n.2167T>G
|
|
|
ENST00000698318.1:n.1950T>G
|
|
|
ENST00000698319.1:n.1313T>G
|
|
|
ENST00000698320.1:n.1201T>G
|
|
|
ENST00000470127.2:n.1214T>G
|
|
|
ENST00000475699.6:c.705T>G
|
ENSP00000419854.3:p.Pro235=
|
|
ENST00000483674.3:n.623T>G
|
|
|
ENST00000601016.6:c.741T>G
MANE Select
|
ENSP00000469981.1:p.Pro247=
|
|
ENST00000612012.5:c.699T>G
|
ENSP00000482070.2:p.Pro233=
|
|
ENST00000612460.5:c.651T>G
|
ENSP00000481037.1:p.Pro217=
|
|
ENST00000614595.2:n.2088T>G
|
|
|
ENST00000615658.5:n.1330T>G
|
|
|
ENST00000616020.5:c.753T>G
|
ENSP00000483636.2:p.Pro251=
|
|
ENST00000617701.5:c.*754T>G
|
ENSP00000481645.1:n.*754T>G
|
|
ENST00000651139.1:c.-43T>G
|
ENSP00000498957.1:n.-43T>G
|
|
ENST00000652354.1:c.423T>G
|
ENSP00000498734.1:p.Pro141=
|
|
ENST00000652358.1:c.534T>G
|
ENSP00000498464.1:p.Pro178=
|
|
ENST00000652390.1:c.660T>G
|
ENSP00000498858.1:p.Pro220=
|
|
ENST00000652476.1:n.1407T>G
|
|
|
ENST00000652644.1:c.354T>G
|
ENSP00000498496.1:p.Pro118=
|
|
ENST00000652682.1:c.798T>G
|
ENSP00000498288.1:p.Pro266=
|
|
ENST00000652685.1:n.1094T>G
|
|
|
ENST00000369776.8:c.651T>G
|
ENSP00000358791.4:p.Pro217=
|
|
ENST00000426231.5:c.738T>G
|
|
|
ENST00000475699.5:c.699T>G
|
ENSP00000419854.2:p.Pro233=
|
|
ENST00000494912.5:n.1430T>G
|
|
|
ENST00000498029.1:n.199T>G
|
|
|
ENST00000601016.5:c.741T>G
|
ENSP00000469981.1:p.Pro247=
|
|
ENST00000612460.4:c.651T>G
|
ENSP00000481037.1:p.Pro217=
|
|
ENST00000613002.4:c.609T>G
|
ENSP00000478154.1:p.Pro203=
|
|
ENST00000615986.4:c.*469T>G
|
ENSP00000480133.1:n.*469T>G
|
|
NM_000116.4:c.741T>G
|
NP_000107.1:p.Pro247=
|
|
NM_001303465.1:c.753T>G
|
NP_001290394.1:p.Pro251=
|
|
NM_181311.3:c.651T>G
|
NP_851828.1:p.Pro217=
|
|
NM_181312.3:c.699T>G
|
NP_851829.1:p.Pro233=
|
|
NM_181313.3:c.609T>G
|
NP_851830.1:p.Pro203=
|
|
NR_024048.2:n.1083T>G
|
|
|
XM_006724836.1:c.795T>G
|
XP_006724899.1:p.Pro265=
|
|
XM_006724837.1:c.780T>G
|
XP_006724900.1:p.Pro260=
|
|
XM_006724839.1:c.663T>G
|
XP_006724902.1:p.Pro221=
|
|
XM_006724841.2:c.534T>G
|
XP_006724904.1:p.Pro178=
|
|
XM_006724842.2:c.444T>G
|
XP_006724905.1:p.Pro148=
|
|
XM_011531189.1:c.582T>G
|
XP_011529491.1:p.Pro194=
|
|
XM_011531190.1:c.534T>G
|
XP_011529492.1:p.Pro178=
|
|
XM_011531191.1:c.465T>G
|
XP_011529493.1:p.Pro155=
|
|
XM_011531192.1:c.462T>G
|
XP_011529494.1:p.Pro154=
|
|
XR_938511.1:n.1089T>G
|
|
|
XM_006724841.4:c.534T>G
|
XP_006724904.1:p.Pro178=
|
|
XM_006724842.4:c.444T>G
|
XP_006724905.1:p.Pro148=
|
|
XM_011531191.2:c.465T>G
|
XP_011529493.1:p.Pro155=
|
|
XM_017029761.1:c.726T>G
|
XP_016885250.1:p.Pro242=
|
|
XM_017029762.1:c.705T>G
|
XP_016885251.1:p.Pro235=
|
|
XM_017029763.1:c.528T>G
|
XP_016885252.1:p.Pro176=
|
|
XM_017029764.1:c.462T>G
|
XP_016885253.1:p.Pro154=
|
|
XM_017029765.2:c.402T>G
|
XP_016885254.1:p.Pro134=
|
|
XM_024452431.1:c.699T>G
|
XP_024308199.1:p.Pro233=
|
|
NM_000116.5:c.741T>G
MANE Select
|
NP_000107.1:p.Pro247=
|
|
NM_001303465.2:c.753T>G
|
NP_001290394.1:p.Pro251=
|
|
NM_181311.4:c.651T>G
|
NP_851828.1:p.Pro217=
|
|
NM_181312.4:c.699T>G
|
NP_851829.1:p.Pro233=
|
|
NM_181313.4:c.609T>G
|
NP_851830.1:p.Pro203=
|
|
NR_024048.3:n.1062T>G
|
|
|