ENST00000696154.2:n.1602G>T
|
|
|
ENST00000696154.1:c.*812G>T
|
ENSP00000512445.1:n.*812G>T
|
|
ENST00000696155.1:n.378G>T
|
|
|
ENST00000259089.9:c.1494G>T
MANE Select
|
ENSP00000259089.4:p.Glu498Asp
|
|
ENST00000645242.1:c.1281G>T
|
ENSP00000494690.1:p.Glu427Asp
|
|
ENST00000259089.8:c.1494G>T
|
ENSP00000259089.4:p.Glu498Asp
|
|
ENST00000526097.1:n.1434G>T
|
|
|
ENST00000529894.1:c.1281G>T
|
ENSP00000433663.1:p.Glu427Asp
|
|
NM_001715.2:c.1494G>T
|
NP_001706.2:p.Glu498Asp
|
|
XM_011543824.1:c.1572G>T
|
XP_011542126.1:p.Glu524Asp
|
|
XM_011543825.1:c.1572G>T
|
XP_011542127.1:p.Glu524Asp
|
|
XM_011543826.1:c.1572G>T
|
XP_011542128.1:p.Glu524Asp
|
|
XM_011543827.1:c.1359G>T
|
XP_011542129.1:p.Glu453Asp
|
|
NM_001330465.1:c.1281G>T
|
NP_001317394.1:p.Glu427Asp
|
|
XM_011543825.3:c.1572G>T
|
XP_011542127.1:p.Glu524Asp
|
|
NM_001715.3:c.1494G>T
MANE Select
|
NP_001706.2:p.Glu498Asp
|
|
NM_001330465.2:c.1281G>T
|
NP_001317394.1:p.Glu427Asp
|
|