ENST00000366835.8:c.1826C>G
MANE Select
|
ENSP00000355800.3:p.Ala609Gly
|
|
ENST00000366835.7:c.1826C>G
|
ENSP00000355800.3:p.Ala609Gly
|
|
NM_014698.2:c.1826C>G
|
NP_055513.2:p.Ala609Gly
|
|
XM_006711841.2:c.1295C>G
|
XP_006711904.1:p.Ala432Gly
|
|
XM_011544328.1:c.1826C>G
|
XP_011542630.1:p.Ala609Gly
|
|
XM_011544329.1:c.1826C>G
|
XP_011542631.1:p.Ala609Gly
|
|
XM_011544330.1:c.1826C>G
|
XP_011542632.1:p.Ala609Gly
|
|
XM_011544331.1:c.1739C>G
|
XP_011542633.1:p.Ala580Gly
|
|
XM_011544332.1:c.1385C>G
|
XP_011542634.1:p.Ala462Gly
|
|
XR_949163.1:n.2131C>G
|
|
|
XM_006711841.4:c.1295C>G
|
XP_006711904.1:p.Ala432Gly
|
|
XM_011544328.3:c.1826C>G
|
XP_011542630.1:p.Ala609Gly
|
|
XM_011544329.3:c.1826C>G
|
XP_011542631.1:p.Ala609Gly
|
|
XM_011544330.3:c.1826C>G
|
XP_011542632.1:p.Ala609Gly
|
|
XM_011544331.3:c.1739C>G
|
XP_011542633.1:p.Ala580Gly
|
|
XM_011544332.3:c.1385C>G
|
XP_011542634.1:p.Ala462Gly
|
|
XR_001737552.2:n.1913C>G
|
|
|
XR_949163.3:n.2110C>G
|
|
|
NM_014698.3:c.1826C>G
MANE Select
|
NP_055513.2:p.Ala609Gly
|
|