|
NM_000088.4:c.3268C>T
MANE Select
|
NP_000079.2:p.Gln1090Ter
|
|
ENST00000225964.10:c.3268C>T
MANE Select
|
ENSP00000225964.6:p.Gln1090Ter
|
|
NM_000088.3:c.3268C>T , LRG_1t1:c.3268C>T
|
NP_000079.2:p.Gln1090Ter
|
|
ENST00000225964.9:c.3268C>T
|
ENSP00000225964.5:p.Gln1090Ter
|
|
ENST00000486572.1:n.466C>T
|
|
|
ENST00000511732.1:n.704C>T
|
|
|
XM_005257058.3:c.2998C>T
|
XP_005257115.2:p.Gln1000Ter
|
|
XM_005257058.4:c.2998C>T
|
XP_005257115.2:p.Gln1000Ter
|
|
XM_005257059.3:c.2350C>T
|
XP_005257116.2:p.Gln784Ter
|
|
XM_005257059.4:c.2350C>T
|
XP_005257116.2:p.Gln784Ter
|
|
XM_011524341.1:c.3070C>T
|
XP_011522643.1:p.Gln1024Ter
|