ENST00000302850.10:c.3208G>T
MANE Select
|
ENSP00000303830.4:p.Glu1070Ter
|
|
ENST00000302850.9:c.3208G>T
|
ENSP00000303830.4:p.Glu1070Ter
|
|
ENST00000341500.9:c.3172G>T
|
ENSP00000342838.4:p.Glu1058Ter
|
|
ENST00000593970.1:n.54G>T
|
|
|
NM_000208.2:c.3208G>T
|
NP_000199.2:p.Glu1070Ter
|
|
NM_000208.3:c.3208G>T
|
NP_000199.2:p.Glu1070Ter
|
|
NM_001079817.1:c.3172G>T
|
NP_001073285.1:p.Glu1058Ter
|
|
NM_001079817.2:c.3172G>T
|
NP_001073285.1:p.Glu1058Ter
|
|
XM_011527988.1:c.3283G>T
|
XP_011526290.1:p.Glu1095Ter
|
|
XM_011527989.1:c.3247G>T
|
XP_011526291.1:p.Glu1083Ter
|
|
XM_011527988.2:c.3205G>T
|
XP_011526290.2:p.Glu1069Ter
|
|
XM_011527989.3:c.3169G>T
|
XP_011526291.2:p.Glu1057Ter
|
|
NM_000208.4:c.3208G>T
MANE Select
|
NP_000199.2:p.Glu1070Ter
|
|
NM_001079817.3:c.3172G>T
|
NP_001073285.1:p.Glu1058Ter
|
|