ENST00000356392.9:c.1156G>A
MANE Select
|
ENSP00000348757.3:p.Ala386Thr
|
|
ENST00000356392.8:c.1156G>A
|
ENSP00000348757.3:p.Ala386Thr
|
|
ENST00000586836.5:c.583G>A
|
ENSP00000467429.1:p.Ala195Thr
|
|
ENST00000591179.5:c.976G>A
|
ENSP00000466800.1:p.Ala326Thr
|
|
ENST00000591345.5:c.*1075G>A
|
ENSP00000467313.1:n.*1075G>A
|
|
NM_001302453.1:c.994G>A
|
NP_001289382.1:p.Ala332Thr
|
|
NM_001302454.1:c.976G>A
|
NP_001289383.1:p.Ala326Thr
|
|
NM_145045.4:c.1156G>A
|
NP_659482.3:p.Ala386Thr
|
|
XM_017026241.1:c.*50G>A
|
XP_016881730.1:n.*50G>A
|
|
NM_145045.5:c.1156G>A
MANE Select
|
NP_659482.3:p.Ala386Thr
|
|
NM_001302454.2:c.976G>A
|
NP_001289383.1:p.Ala326Thr
|
|