|
NM_145045.5:c.487C>T
MANE Select
|
NP_659482.3:p.Gln163Ter
|
|
ENST00000356392.9:c.487C>T
MANE Select
|
ENSP00000348757.3:p.Gln163Ter
|
|
NM_001302453.1:c.325C>T
|
NP_001289382.1:p.Gln109Ter
|
|
NM_001302454.1:c.409C>T
|
NP_001289383.1:p.Gln137Ter
|
|
NM_001302454.2:c.409C>T
|
NP_001289383.1:p.Gln137Ter
|
|
NM_145045.4:c.487C>T
|
NP_659482.3:p.Gln163Ter
|
|
ENST00000356392.8:c.487C>T
|
ENSP00000348757.3:p.Gln163Ter
|
|
ENST00000586836.5:c.-87C>T
|
ENSP00000467429.1:n.-87C>T
|
|
ENST00000591179.5:c.409C>T
|
ENSP00000466800.1:p.Gln137Ter
|
|
ENST00000591345.5:c.*406C>T
|
ENSP00000467313.1:n.*406C>T
|
|
XM_017026241.1:c.487C>T
|
XP_016881730.1:p.Gln163Ter
|