ENST00000355699.7:c.2840A>G
MANE Select
|
ENSP00000347927.2:p.Gln947Arg
|
|
ENST00000355699.6:c.2840A>G
|
ENSP00000347927.2:p.Gln947Arg
|
|
ENST00000356589.6:c.2747A>G
|
ENSP00000348997.2:p.Gln916Arg
|
|
ENST00000371916.5:c.*309A>G
|
ENSP00000360984.2:n.*309A>G
|
|
ENST00000371929.7:c.2840A>G
|
ENSP00000360997.3:p.Gln947Arg
|
|
ENST00000485925.5:n.1656A>G
|
|
|
ENST00000495234.5:c.*1672A>G
|
ENSP00000435274.1:n.*1672A>G
|
|
NM_139025.4:c.2840A>G , LRG_544t1:c.2840A>G
|
NP_620594.1:p.Gln947Arg
|
|
NM_139026.4:c.2747A>G
|
NP_620595.1:p.Gln916Arg
|
|
NM_139027.4:c.2840A>G
|
NP_620596.2:p.Gln947Arg
|
|
NR_024514.2:n.1675A>G
|
|
|
XM_011518174.1:c.2450A>G
|
XP_011516476.1:p.Gln817Arg
|
|
XM_011518175.1:c.2840A>G
|
XP_011516477.1:p.Gln947Arg
|
|
XM_011518176.1:c.1856A>G
|
XP_011516478.1:p.Gln619Arg
|
|
XM_011518177.1:c.1850A>G
|
XP_011516479.1:p.Gln617Arg
|
|
XM_011518178.1:c.1505A>G
|
XP_011516480.1:p.Gln502Arg
|
|
XM_011518179.1:c.1505A>G
|
XP_011516481.1:p.Gln502Arg
|
|
XM_011518180.1:c.1106A>G
|
XP_011516482.1:p.Gln369Arg
|
|
XM_011518176.3:c.1856A>G
|
XP_011516478.1:p.Gln619Arg
|
|
XM_011518178.2:c.1505A>G
|
XP_011516480.1:p.Gln502Arg
|
|
XM_017014232.1:c.2828A>G
|
XP_016869721.1:p.Gln943Arg
|
|
XM_017014233.1:c.2450A>G
|
XP_016869722.1:p.Gln817Arg
|
|
XM_017014234.2:c.1850A>G
|
XP_016869723.1:p.Gln617Arg
|
|
XR_001746171.1:n.3613A>G
|
|
|
NM_139026.5:c.2747A>G
|
NP_620595.1:p.Gln916Arg
|
|
NM_139027.5:c.2840A>G
|
NP_620596.2:p.Gln947Arg
|
|
NM_139025.5:c.2840A>G
|
NP_620594.1:p.Gln947Arg
|
|
NM_139026.6:c.2747A>G
|
NP_620595.1:p.Gln916Arg
|
|
NM_139027.6:c.2840A>G
MANE Select
|
NP_620596.2:p.Gln947Arg
|
|
NR_024514.3:n.1677A>G
|
|
|