ENST00000554752.7:c.*2943G>T
MANE Select
|
ENSP00000451612.2:n.*2943G>T
|
|
ENST00000554752.6:c.6258G>T
|
ENSP00000451612.2:n.6258G>T
|
|
ENST00000611979.4:c.5586G>T
|
ENSP00000480011.1:n.5586G>T
|
|
NM_001284230.1:c.6258G>T
|
NP_001271159.1:n.6258G>T
|
|
NM_001284231.1:c.*2943G>T
|
NP_001271160.1:n.*2943G>T
|
|
NM_001284232.1:c.*2943G>T
|
NP_001271161.1:n.*2943G>T
|
|
NM_033141.3:c.6300G>T
|
NP_149132.2:n.6300G>T
|
|
XM_005267683.3:c.*2943G>T
|
XP_005267740.1:n.*2943G>T
|
|
XM_011536788.1:c.*2943G>T
|
XP_011535090.1:n.*2943G>T
|
|
XM_011536789.1:c.*2943G>T
|
XP_011535091.1:n.*2943G>T
|
|
XM_011536790.1:c.*2943G>T
|
XP_011535092.1:n.*2943G>T
|
|
XM_011536791.1:c.*2943G>T
|
XP_011535093.1:n.*2943G>T
|
|
XM_011536792.1:c.*2943G>T
|
XP_011535094.1:n.*2943G>T
|
|
XM_011536793.1:c.*2943G>T
|
XP_011535095.1:n.*2943G>T
|
|
XM_011536794.1:c.*2943G>T
|
XP_011535096.1:n.*2943G>T
|
|
XM_005267683.5:c.*2943G>T
|
XP_005267740.1:n.*2943G>T
|
|
XM_011536788.3:c.*2943G>T
|
XP_011535090.1:n.*2943G>T
|
|
XM_011536794.2:c.*2943G>T
|
XP_011535096.1:n.*2943G>T
|
|
NM_033141.4:c.*2943G>T
|
NP_149132.2:n.*2943G>T
|
|
NM_001284230.2:c.*2943G>T
MANE Select
|
NP_001271159.1:n.*2943G>T
|
|