ENST00000710359.1:c.4456G=
|
ENSP00000518230.1:p.Glu1486=
|
|
ENST00000379802.8:c.5785G=
MANE Select
|
ENSP00000369129.3:p.Glu1929=
|
|
ENST00000379802.7:c.5785G=
|
ENSP00000369129.3:p.Glu1929=
|
|
ENST00000418664.2:c.3988G=
|
ENSP00000396591.2:p.Glu1330=
|
|
NM_001008844.1:c.3988G=
|
NP_001008844.1:p.Glu1330=
|
|
NM_004415.2:c.5785G= , LRG_423t1:c.5785G=
|
NP_004406.2:p.Glu1929=
|
|
XM_011514323.1:c.4456G=
|
XP_011512625.1:p.Glu1486=
|
|
NM_001008844.2:c.3988G=
|
NP_001008844.1:p.Glu1330=
|
|
NM_001319034.1:c.4456G=
|
NP_001305963.1:p.Glu1486=
|
|
NM_004415.3:c.5785G=
|
NP_004406.2:p.Glu1929=
|
|
NM_004415.4:c.5785G=
MANE Select
|
NP_004406.2:p.Glu1929=
|
|
NM_001008844.3:c.3988G=
|
NP_001008844.1:p.Glu1330=
|
|
NM_001319034.2:c.4456G=
|
NP_001305963.1:p.Glu1486=
|
|