|
NM_005255.4:c.3891C>T
MANE Select
|
NP_005246.2:p.Asp1297=
|
|
ENST00000314167.9:c.3891C>T
MANE Select
|
ENSP00000314499.4:p.Asp1297=
|
|
NM_001286833.1:c.3597C>T
|
NP_001273762.1:p.Asp1199=
|
|
NM_001318134.1:c.3654C>T
|
NP_001305063.1:p.Asp1218=
|
|
NM_001318134.2:c.3654C>T
|
NP_001305063.1:p.Asp1218=
|
|
NM_005255.2:c.3891C>T
|
NP_005246.2:p.Asp1297=
|
|
NM_005255.3:c.3891C>T
|
NP_005246.2:p.Asp1297=
|
|
ENST00000314167.8:c.3891C>T
|
ENSP00000314499.4:p.Asp1297=
|
|
ENST00000502799.1:n.1839C>T
|
|
|
ENST00000504668.5:c.488C>T
|
ENSP00000424553.1:n.488C>T
|
|
ENST00000509566.1:n.2686C>T
|
|
|
ENST00000511163.5:c.3654C>T
|
ENSP00000421361.1:p.Asp1218=
|
|
ENST00000511345.5:n.3127C>T
|
|
|
ENST00000511980.5:c.1358C>T
|
|
|
ENST00000515868.5:n.3463C>T
|
|
|
ENST00000618573.4:c.1206C>T
|
ENSP00000484475.1:p.Asp402=
|
|
XM_005272268.1:c.3858C>T
|
XP_005272325.1:p.Asp1286=
|
|
XM_005272268.2:c.3858C>T
|
XP_005272325.1:p.Asp1286=
|
|
XM_005272270.1:c.3666C>T
|
XP_005272327.1:p.Asp1222=
|
|
XM_005272270.2:c.3666C>T
|
XP_005272327.1:p.Asp1222=
|
|
XM_011513425.1:c.4023C>T
|
XP_011511727.1:p.Asp1341=
|
|
XM_011513425.2:c.4023C>T
|
XP_011511727.1:p.Asp1341=
|
|
XM_011513426.1:c.3990C>T
|
XP_011511728.1:p.Asp1330=
|
|
XM_011513426.2:c.3990C>T
|
XP_011511728.1:p.Asp1330=
|
|
XM_011513427.1:c.3933C>T
|
XP_011511729.1:p.Asp1311=
|
|
XM_011513427.2:c.3933C>T
|
XP_011511729.1:p.Asp1311=
|
|
XM_011513428.1:c.3876C>T
|
XP_011511730.1:p.Asp1292=
|
|
XM_011513428.2:c.3876C>T
|
XP_011511730.1:p.Asp1292=
|
|
XM_011513429.1:c.3837C>T
|
XP_011511731.1:p.Asp1279=
|
|
XM_011513429.2:c.3837C>T
|
XP_011511731.1:p.Asp1279=
|
|
XM_011513430.1:c.3786C>T
|
XP_011511732.1:p.Asp1262=
|
|
XM_011513431.1:c.3774C>T
|
XP_011511733.1:p.Asp1258=
|
|
XM_011513431.2:c.3774C>T
|
XP_011511733.1:p.Asp1258=
|
|
XM_011513432.1:c.3759C>T
|
XP_011511734.1:p.Asp1253=
|
|
XM_011513432.2:c.3759C>T
|
XP_011511734.1:p.Asp1253=
|
|
XM_011513433.1:c.3654C>T
|
XP_011511735.1:p.Asp1218=
|
|
XM_011513434.1:c.3615C>T
|
XP_011511736.1:p.Asp1205=
|
|
XM_011513434.2:c.3615C>T
|
XP_011511736.1:p.Asp1205=
|
|
XM_017007991.1:c.3801C>T
|
XP_016863480.1:p.Asp1267=
|
|
XM_017007992.1:c.3696C>T
|
XP_016863481.1:p.Asp1232=
|
|
XM_017007993.1:c.3615C>T
|
XP_016863482.1:p.Asp1205=
|
|
XM_017007995.1:c.3351C>T
|
XP_016863484.1:p.Asp1117=
|
