ENST00000298910.12:c.5982C>T
MANE Select
|
ENSP00000298910.7:p.Asp1994=
|
|
ENST00000679360.1:c.*4891C>T
|
ENSP00000505368.1:n.*4891C>T
|
|
ENST00000679532.1:c.1756C>T
|
|
|
ENST00000680018.1:c.1427C>T
|
ENSP00000505347.1:n.1427C>T
|
|
ENST00000680422.1:c.1627C>T
|
|
|
ENST00000680425.1:c.1149C>T
|
ENSP00000506459.1:n.1149C>T
|
|
ENST00000680453.1:c.1439C>T
|
|
|
ENST00000680790.1:c.5727C>T
|
ENSP00000505335.1:p.Asp1909=
|
|
ENST00000681136.1:n.1966C>T
|
|
|
ENST00000681696.1:c.1665C>T
|
ENSP00000505871.1:p.Asp555=
|
|
ENST00000298910.11:c.5982C>T
|
ENSP00000298910.7:p.Asp1994=
|
|
ENST00000430804.5:c.3278C>T
|
|
|
ENST00000479187.5:n.2663C>T
|
|
|
NM_198578.3:c.5982C>T
|
NP_940980.3:p.Asp1994=
|
|
XM_005268629.2:c.5982C>T
|
XP_005268686.1:p.Asp1994=
|
|
XM_011537877.1:c.5982C>T
|
XP_011536179.1:p.Asp1994=
|
|
XM_011537878.1:c.5982C>T
|
XP_011536180.1:p.Asp1994=
|
|
XM_011537879.1:c.4779C>T
|
XP_011536181.1:p.Asp1593=
|
|
XM_005268629.4:c.5982C>T
|
XP_005268686.1:p.Asp1994=
|
|
XM_011537877.3:c.5982C>T
|
XP_011536179.1:p.Asp1994=
|
|
XM_017018787.1:c.2898C>T
|
XP_016874276.1:p.Asp966=
|
|
XM_017018788.2:c.2244C>T
|
XP_016874277.1:p.Asp748=
|
|
XM_024448833.1:c.4779C>T
|
XP_024304601.1:p.Asp1593=
|
|
NM_198578.4:c.5982C>T
MANE Select
|
NP_940980.4:p.Asp1994=
|
|