ENST00000225964.10:c.4152C>G
MANE Select
|
ENSP00000225964.6:p.Leu1384=
|
|
ENST00000225964.9:c.4152C>G
|
ENSP00000225964.5:p.Leu1384=
|
|
ENST00000510710.3:n.1117C>G
|
|
|
NM_000088.3:c.4152C>G , LRG_1t1:c.4152C>G
|
NP_000079.2:p.Leu1384=
|
|
XM_005257058.3:c.3882C>G
|
XP_005257115.2:p.Leu1294=
|
|
XM_005257059.3:c.3234C>G
|
XP_005257116.2:p.Leu1078=
|
|
XM_011524341.1:c.3954C>G
|
XP_011522643.1:p.Leu1318=
|
|
XM_005257058.4:c.3882C>G
|
XP_005257115.2:p.Leu1294=
|
|
XM_005257059.4:c.3234C>G
|
XP_005257116.2:p.Leu1078=
|
|
NM_000088.4:c.4152C>G
MANE Select
|
NP_000079.2:p.Leu1384=
|
|