ENST00000225964.10:c.3163G>C
MANE Select
|
ENSP00000225964.6:p.Gly1055Arg
|
|
ENST00000225964.9:c.3163G>C
|
ENSP00000225964.5:p.Gly1055Arg
|
|
ENST00000511732.1:n.107G>C
|
|
|
NM_000088.3:c.3163G>C , LRG_1t1:c.3163G>C
|
NP_000079.2:p.Gly1055Arg
|
|
XM_005257058.3:c.2893G>C
|
XP_005257115.2:p.Gly965Arg
|
|
XM_005257059.3:c.2245G>C
|
XP_005257116.2:p.Gly749Arg
|
|
XM_011524341.1:c.2965G>C
|
XP_011522643.1:p.Gly989Arg
|
|
XM_005257058.4:c.2893G>C
|
XP_005257115.2:p.Gly965Arg
|
|
XM_005257059.4:c.2245G>C
|
XP_005257116.2:p.Gly749Arg
|
|
NM_000088.4:c.3163G>C
MANE Select
|
NP_000079.2:p.Gly1055Arg
|
|