ENST00000356392.9:c.1329G>T
MANE Select
|
ENSP00000348757.3:p.Arg443=
|
|
ENST00000356392.8:c.1329G>T
|
ENSP00000348757.3:p.Arg443=
|
|
ENST00000586836.5:c.756G>T
|
ENSP00000467429.1:p.Arg252=
|
|
ENST00000591179.5:c.1149G>T
|
ENSP00000466800.1:p.Arg383=
|
|
ENST00000591345.5:c.*1248G>T
|
ENSP00000467313.1:n.*1248G>T
|
|
NM_001302453.1:c.1167G>T
|
NP_001289382.1:p.Arg389=
|
|
NM_001302454.1:c.1149G>T
|
NP_001289383.1:p.Arg383=
|
|
NM_145045.4:c.1329G>T
|
NP_659482.3:p.Arg443=
|
|
NM_145045.5:c.1329G>T
MANE Select
|
NP_659482.3:p.Arg443=
|
|
NM_001302454.2:c.1149G>T
|
NP_001289383.1:p.Arg383=
|
|