ENST00000225964.10:c.4174G>C
MANE Select
|
ENSP00000225964.6:p.Gly1392Arg
|
|
ENST00000225964.9:c.4174G>C
|
ENSP00000225964.5:p.Gly1392Arg
|
|
ENST00000510710.3:n.1139G>C
|
|
|
NM_000088.3:c.4174G>C , LRG_1t1:c.4174G>C
|
NP_000079.2:p.Gly1392Arg
|
|
XM_005257058.3:c.3904G>C
|
XP_005257115.2:p.Gly1302Arg
|
|
XM_005257059.3:c.3256G>C
|
XP_005257116.2:p.Gly1086Arg
|
|
XM_011524341.1:c.3976G>C
|
XP_011522643.1:p.Gly1326Arg
|
|
XM_005257058.4:c.3904G>C
|
XP_005257115.2:p.Gly1302Arg
|
|
XM_005257059.4:c.3256G>C
|
XP_005257116.2:p.Gly1086Arg
|
|
NM_000088.4:c.4174G>C
MANE Select
|
NP_000079.2:p.Gly1392Arg
|
|