ENST00000356392.9:c.1279C>T
MANE Select
|
ENSP00000348757.3:p.Gln427Ter
|
|
ENST00000356392.8:c.1279C>T
|
ENSP00000348757.3:p.Gln427Ter
|
|
ENST00000586836.5:c.706C>T
|
ENSP00000467429.1:p.Gln236Ter
|
|
ENST00000591179.5:c.1099C>T
|
ENSP00000466800.1:p.Gln367Ter
|
|
ENST00000591345.5:c.*1198C>T
|
ENSP00000467313.1:n.*1198C>T
|
|
NM_001302453.1:c.1117C>T
|
NP_001289382.1:p.Gln373Ter
|
|
NM_001302454.1:c.1099C>T
|
NP_001289383.1:p.Gln367Ter
|
|
NM_145045.4:c.1279C>T
|
NP_659482.3:p.Gln427Ter
|
|
NM_145045.5:c.1279C>T
MANE Select
|
NP_659482.3:p.Gln427Ter
|
|
NM_001302454.2:c.1099C>T
|
NP_001289383.1:p.Gln367Ter
|
|