ENST00000449082.3:c.1696G>T
MANE Select
|
ENSP00000390600.2:p.Glu566Ter
|
|
ENST00000643924.1:c.1696G>T
|
ENSP00000495595.1:p.Glu566Ter
|
|
ENST00000655275.1:c.1723G>T
|
ENSP00000499510.1:p.Glu575Ter
|
|
ENST00000449082.2:c.1696G>T
|
ENSP00000390600.2:p.Glu566Ter
|
|
NM_001293306.2:c.1696G>T
|
NP_001280235.2:p.Glu566Ter
|
|
NM_001293307.2:c.1462-2094G>T
|
NP_001280236.2:n.1462-2094G>T
|
|
NM_006514.3:c.1696G>T
|
NP_006505.3:p.Glu566Ter
|
|
XM_005265371.2:c.1705G>T
|
XP_005265428.1:p.Glu569Ter
|
|
XM_011533993.1:c.1705G>T
|
XP_011532295.1:p.Glu569Ter
|
|
XM_011533994.1:c.1471-2094G>T
|
XP_011532296.1:n.1471-2094G>T
|
|
XM_005265371.3:c.1705G>T
|
XP_005265428.1:p.Glu569Ter
|
|
XM_011533993.2:c.1705G>T
|
XP_011532295.1:p.Glu569Ter
|
|
XM_011533994.2:c.1471-2094G>T
|
XP_011532296.1:n.1471-2094G>T
|
|
NM_006514.4:c.1696G>T
MANE Select
|
NP_006505.4:p.Glu566Ter
|
|