ENST00000225964.10:c.3443G>A
MANE Select
|
ENSP00000225964.6:p.Gly1148Asp
|
|
ENST00000225964.9:c.3443G>A
|
ENSP00000225964.5:p.Gly1148Asp
|
|
ENST00000510710.3:n.20G>A
|
|
|
NM_000088.3:c.3443G>A , LRG_1t1:c.3443G>A
|
NP_000079.2:p.Gly1148Asp
|
|
XM_005257058.3:c.3173G>A
|
XP_005257115.2:p.Gly1058Asp
|
|
XM_005257059.3:c.2525G>A
|
XP_005257116.2:p.Gly842Asp
|
|
XM_011524341.1:c.3245G>A
|
XP_011522643.1:p.Gly1082Asp
|
|
XM_005257058.4:c.3173G>A
|
XP_005257115.2:p.Gly1058Asp
|
|
XM_005257059.4:c.2525G>A
|
XP_005257116.2:p.Gly842Asp
|
|
NM_000088.4:c.3443G>A
MANE Select
|
NP_000079.2:p.Gly1148Asp
|
|