|
ENST00000377838.8:c.1193G>T
MANE Select
|
ENSP00000367069.3:p.Gly398Val
|
|
|
ENST00000377838.7:c.1193G>T
|
ENSP00000367069.3:p.Gly398Val
|
|
|
ENST00000429442.6:c.1157G>T
|
ENSP00000394501.2:p.Gly386Val
|
|
|
ENST00000520214.5:c.1157G>T
|
ENSP00000428483.1:p.Gly386Val
|
|
|
ENST00000520356.5:c.1157G>T
|
ENSP00000427879.1:p.Gly386Val
|
|
|
ENST00000520727.5:c.1157G>T
|
ENSP00000427831.1:p.Gly386Val
|
|
|
ENST00000522974.5:n.1298G>T
|
|
|
|
ENST00000523243.5:c.1193G>T
|
ENSP00000429930.1:p.Gly398Val
|
|
|
ENST00000523399.5:c.1007G>T
|
ENSP00000429091.1:p.Gly336Val
|
|
|
ENST00000523924.5:c.*1175G>T
|
ENSP00000429050.1:n.*1175G>T
|
|
|
NM_001029939.3:c.1157G>T
|
NP_001025110.2:p.Gly386Val
|
|
|
NM_001167583.2:c.1157G>T
|
NP_001161055.1:p.Gly386Val
|
|
|
NM_001174157.1:c.1007G>T
|
NP_001167628.1:p.Gly336Val
|
|
|
NM_001174158.1:c.1157G>T
|
NP_001167629.1:p.Gly386Val
|
|
|
NM_001289394.1:c.1157G>T
|
NP_001276323.1:p.Gly386Val
|
|
|
NM_020863.3:c.1193G>T
|
NP_065914.2:p.Gly398Val
|
|
|
NR_110323.1:n.1379G>T
|
|
|
|
XM_011517203.1:c.1157G>T
|
XP_011515505.1:p.Gly386Val
|
|
|
XM_011517204.1:c.1007G>T
|
XP_011515506.1:p.Gly336Val
|
|
|
XM_011517205.1:c.1157G>T
|
XP_011515507.1:p.Gly386Val
|
|
|
XM_011517206.1:c.1157G>T
|
XP_011515508.1:p.Gly386Val
|
|
|
XR_928343.1:n.1174G>T
|
|
|
|
XM_011517204.2:c.1007G>T
|
XP_011515506.1:p.Gly336Val
|
|
|
XM_011517206.2:c.1157G>T
|
XP_011515508.1:p.Gly386Val
|
|
|
XM_017013716.1:c.1157G>T
|
XP_016869205.1:p.Gly386Val
|
|
|
XR_001745568.1:n.1174G>T
|
|
|
|
XR_001745569.1:n.1174G>T
|
|
|
|
XR_001745570.1:n.1174G>T
|
|
|
|
XR_928343.2:n.1174G>T
|
|
|
|
NM_020863.4:c.1193G>T
MANE Select
|
NP_065914.2:p.Gly398Val
|
|
|
NM_001029939.4:c.1157G>T
|
NP_001025110.2:p.Gly386Val
|
|
|
NM_001167583.3:c.1157G>T
|
NP_001161055.1:p.Gly386Val
|
|
|
NM_001174157.2:c.1007G>T
|
NP_001167628.1:p.Gly336Val
|
|
|
NM_001174158.2:c.1157G>T
|
NP_001167629.1:p.Gly386Val
|
|
|
NM_001289394.2:c.1157G>T
|
NP_001276323.1:p.Gly386Val
|
|
|
NR_110323.2:n.1361G>T
|
|
|
