ENST00000333646.11:c.1746G>T
|
ENSP00000333125.8:p.Arg582Ser
|
|
ENST00000374102.6:c.1866G>T
|
ENSP00000363215.2:p.Gly622=
|
|
ENST00000686548.1:c.*1762G>T
|
ENSP00000509582.1:n.*1762G>T
|
|
ENST00000687382.1:c.1866G>T
|
ENSP00000510724.1:p.Gly622=
|
|
ENST00000688663.1:c.1866G>T
|
ENSP00000509348.1:p.Gly622=
|
|
ENST00000689008.1:c.*2200G>T
|
ENSP00000509134.1:n.*2200G>T
|
|
ENST00000689768.1:n.476G>T
|
|
|
ENST00000690145.1:c.1866G>T
|
ENSP00000508818.1:p.Gly622=
|
|
ENST00000690242.1:c.1866G>T
|
ENSP00000510090.1:p.Gly622=
|
|
ENST00000690828.1:n.2022G>T
|
|
|
ENST00000691385.1:n.1144G>T
|
|
|
ENST00000691426.1:n.97G>T
|
|
|
ENST00000691468.1:c.1866G>T
|
ENSP00000509011.1:p.Gly622=
|
|
ENST00000692304.1:c.1866G>T
|
ENSP00000508427.1:p.Gly622=
|
|
ENST00000692864.1:c.*2200G>T
|
ENSP00000510321.1:n.*2200G>T
|
|
ENST00000693324.1:c.1866G>T
|
ENSP00000508643.1:p.Gly622=
|
|
ENST00000374080.8:c.1866G>T
MANE Select
|
ENSP00000363193.3:p.Gly622=
|
|
ENST00000333646.10:c.1407G>T
|
ENSP00000333125.7:p.Gly469=
|
|
ENST00000374080.7:c.1866G>T
|
ENSP00000363193.3:p.Gly622=
|
|
ENST00000374102.5:c.1866G>T
|
ENSP00000363215.1:p.Gly622=
|
|
NM_005120.2:c.1866G>T
|
NP_005111.2:p.Gly622=
|
|
XM_005262317.1:c.1866G>T
|
XP_005262374.1:p.Gly622=
|
|
XM_005262319.1:c.1866G>T
|
XP_005262376.1:p.Gly622=
|
|
NM_005120.3:c.1866G>T
MANE Select
|
NP_005111.2:p.Gly622=
|
|