NM_000088.4:c.3897C=
MANE Select
|
NP_000079.2:p.Cys1299=
|
ENST00000225964.10:c.3897C=
MANE Select
|
ENSP00000225964.6:p.Cys1299=
|
NM_000088.3:c.3897C= , LRG_1t1:c.3897C=
|
NP_000079.2:p.Cys1299=
|
ENST00000225964.9:c.3897C=
|
ENSP00000225964.5:p.Cys1299=
|
ENST00000510710.3:n.566C=
|
|
XM_005257058.3:c.3627C=
|
XP_005257115.2:p.Cys1209=
|
XM_005257058.4:c.3627C=
|
XP_005257115.2:p.Cys1209=
|
XM_005257059.3:c.2979C=
|
XP_005257116.2:p.Cys993=
|
XM_005257059.4:c.2979C=
|
XP_005257116.2:p.Cys993=
|
XM_011524341.1:c.3699C=
|
XP_011522643.1:p.Cys1233=
|