ENST00000356392.9:c.1169C>T
MANE Select
|
ENSP00000348757.3:p.Thr390Met
|
|
ENST00000356392.8:c.1169C>T
|
ENSP00000348757.3:p.Thr390Met
|
|
ENST00000586836.5:c.596C>T
|
ENSP00000467429.1:p.Thr199Met
|
|
ENST00000591179.5:c.989C>T
|
ENSP00000466800.1:p.Thr330Met
|
|
ENST00000591345.5:c.*1088C>T
|
ENSP00000467313.1:n.*1088C>T
|
|
NM_001302453.1:c.1007C>T
|
NP_001289382.1:p.Thr336Met
|
|
NM_001302454.1:c.989C>T
|
NP_001289383.1:p.Thr330Met
|
|
NM_145045.4:c.1169C>T
|
NP_659482.3:p.Thr390Met
|
|
XM_017026241.1:c.*63C>T
|
XP_016881730.1:n.*63C>T
|
|
NM_145045.5:c.1169C>T
MANE Select
|
NP_659482.3:p.Thr390Met
|
|
NM_001302454.2:c.989C>T
|
NP_001289383.1:p.Thr330Met
|
|