ENST00000225964.10:c.3496G>A
MANE Select
|
ENSP00000225964.6:p.Gly1166Ser
|
|
ENST00000225964.9:c.3496G>A
|
ENSP00000225964.5:p.Gly1166Ser
|
|
ENST00000510710.3:n.73G>A
|
|
|
NM_000088.3:c.3496G>A , LRG_1t1:c.3496G>A
|
NP_000079.2:p.Gly1166Ser
|
|
XM_005257058.3:c.3226G>A
|
XP_005257115.2:p.Gly1076Ser
|
|
XM_005257059.3:c.2578G>A
|
XP_005257116.2:p.Gly860Ser
|
|
XM_011524341.1:c.3298G>A
|
XP_011522643.1:p.Gly1100Ser
|
|
XM_005257058.4:c.3226G>A
|
XP_005257115.2:p.Gly1076Ser
|
|
XM_005257059.4:c.2578G>A
|
XP_005257116.2:p.Gly860Ser
|
|
NM_000088.4:c.3496G>A
MANE Select
|
NP_000079.2:p.Gly1166Ser
|
|