ENST00000225964.10:c.4200C>G
MANE Select
|
ENSP00000225964.6:p.Ala1400=
|
|
ENST00000225964.9:c.4200C>G
|
ENSP00000225964.5:p.Ala1400=
|
|
NM_000088.3:c.4200C>G , LRG_1t1:c.4200C>G
|
NP_000079.2:p.Ala1400=
|
|
XM_005257058.3:c.3930C>G
|
XP_005257115.2:p.Ala1310=
|
|
XM_005257059.3:c.3282C>G
|
XP_005257116.2:p.Ala1094=
|
|
XM_011524341.1:c.4002C>G
|
XP_011522643.1:p.Ala1334=
|
|
XM_005257058.4:c.3930C>G
|
XP_005257115.2:p.Ala1310=
|
|
XM_005257059.4:c.3282C>G
|
XP_005257116.2:p.Ala1094=
|
|
NM_000088.4:c.4200C>G
MANE Select
|
NP_000079.2:p.Ala1400=
|
|