ENST00000265471.10:c.754G>T
MANE Select
|
ENSP00000265471.5:p.Asp252Tyr
|
|
ENST00000265471.9:c.754G>T
|
ENSP00000265471.5:p.Asp252Tyr
|
|
ENST00000531383.5:c.754G>T
|
ENSP00000431359.1:p.Asp252Tyr
|
|
ENST00000532585.5:c.*876G>T
|
ENSP00000432604.1:n.*876G>T
|
|
ENST00000534026.5:c.754G>T
|
ENSP00000432474.1:p.Asp252Tyr
|
|
NM_001288721.1:c.733G>T
|
NP_001275650.1:p.Asp245Tyr
|
|
NM_001288722.1:c.754G>T
|
NP_001275651.1:p.Asp252Tyr
|
|
NM_001288723.1:c.754G>T
|
NP_001275652.1:p.Asp252Tyr
|
|
NM_012200.3:c.754G>T
|
NP_036332.2:p.Asp252Tyr
|
|
NR_109991.1:n.972G>T
|
|
|
XM_011544936.1:c.733G>T
|
XP_011543238.1:p.Asp245Tyr
|
|
NM_012200.4:c.754G>T
MANE Select
|
NP_036332.2:p.Asp252Tyr
|
|
NM_001288721.2:c.733G>T
|
NP_001275650.1:p.Asp245Tyr
|
|
NM_001288722.2:c.754G>T
|
NP_001275651.1:p.Asp252Tyr
|
|
NM_001288723.2:c.754G>T
|
NP_001275652.1:p.Asp252Tyr
|
|
NR_109991.2:n.783G>T
|
|
|