ENST00000356392.9:c.1202G>T
MANE Select
|
ENSP00000348757.3:p.Arg401Met
|
|
ENST00000356392.8:c.1202G>T
|
ENSP00000348757.3:p.Arg401Met
|
|
ENST00000586836.5:c.629G>T
|
ENSP00000467429.1:p.Arg210Met
|
|
ENST00000591179.5:c.1022G>T
|
ENSP00000466800.1:p.Arg341Met
|
|
ENST00000591345.5:c.*1121G>T
|
ENSP00000467313.1:n.*1121G>T
|
|
NM_001302453.1:c.1040G>T
|
NP_001289382.1:p.Arg347Met
|
|
NM_001302454.1:c.1022G>T
|
NP_001289383.1:p.Arg341Met
|
|
NM_145045.4:c.1202G>T
|
NP_659482.3:p.Arg401Met
|
|
NM_145045.5:c.1202G>T
MANE Select
|
NP_659482.3:p.Arg401Met
|
|
NM_001302454.2:c.1022G>T
|
NP_001289383.1:p.Arg341Met
|
|