ENST00000356392.9:c.1152C>T
MANE Select
|
ENSP00000348757.3:p.Thr384=
|
|
ENST00000356392.8:c.1152C>T
|
ENSP00000348757.3:p.Thr384=
|
|
ENST00000586836.5:c.579C>T
|
ENSP00000467429.1:p.Thr193=
|
|
ENST00000591179.5:c.972C>T
|
ENSP00000466800.1:p.Thr324=
|
|
ENST00000591345.5:c.*1071C>T
|
ENSP00000467313.1:n.*1071C>T
|
|
NM_001302453.1:c.990C>T
|
NP_001289382.1:p.Thr330=
|
|
NM_001302454.1:c.972C>T
|
NP_001289383.1:p.Thr324=
|
|
NM_145045.4:c.1152C>T
|
NP_659482.3:p.Thr384=
|
|
XM_017026241.1:c.*46C>T
|
XP_016881730.1:n.*46C>T
|
|
NM_145045.5:c.1152C>T
MANE Select
|
NP_659482.3:p.Thr384=
|
|
NM_001302454.2:c.972C>T
|
NP_001289383.1:p.Thr324=
|
|