ENST00000356392.9:c.1141C>T
MANE Select
|
ENSP00000348757.3:p.Gln381Ter
|
|
ENST00000356392.8:c.1141C>T
|
ENSP00000348757.3:p.Gln381Ter
|
|
ENST00000586836.5:c.568C>T
|
ENSP00000467429.1:p.Gln190Ter
|
|
ENST00000591179.5:c.961C>T
|
ENSP00000466800.1:p.Gln321Ter
|
|
ENST00000591345.5:c.*1060C>T
|
ENSP00000467313.1:n.*1060C>T
|
|
NM_001302453.1:c.979C>T
|
NP_001289382.1:p.Gln327Ter
|
|
NM_001302454.1:c.961C>T
|
NP_001289383.1:p.Gln321Ter
|
|
NM_145045.4:c.1141C>T
|
NP_659482.3:p.Gln381Ter
|
|
XM_017026241.1:c.*35C>T
|
XP_016881730.1:n.*35C>T
|
|
NM_145045.5:c.1141C>T
MANE Select
|
NP_659482.3:p.Gln381Ter
|
|
NM_001302454.2:c.961C>T
|
NP_001289383.1:p.Gln321Ter
|
|