ENST00000222214.10:c.1212C>G
MANE Select
|
ENSP00000222214.4:p.Ala404=
|
|
ENST00000222214.9:c.1212C>G
|
ENSP00000222214.4:p.Ala404=
|
|
ENST00000585420.5:n.1542C>G
|
|
|
ENST00000590472.5:c.256C>G
|
|
|
ENST00000590530.5:c.*652C>G
|
ENSP00000468452.1:n.*652C>G
|
|
ENST00000591043.1:n.1522C>G
|
|
|
ENST00000591050.1:c.179C>G
|
|
|
ENST00000591470.5:c.1212C>G
|
ENSP00000466845.1:p.Ala404=
|
|
NM_000159.3:c.1212C>G
|
NP_000150.1:p.Ala404=
|
|
NM_013976.3:c.1212C>G
|
NP_039663.1:p.Ala404=
|
|
NR_102316.1:n.1375C>G
|
|
|
NR_102317.1:n.1593C>G
|
|
|
XM_006722721.2:c.1212C>G
|
XP_006722784.1:p.Ala404=
|
|
XM_011527899.1:c.1212C>G
|
XP_011526201.1:p.Ala404=
|
|
XM_011527900.1:c.1212C>G
|
XP_011526202.1:p.Ala404=
|
|
XM_011527899.2:c.1212C>G
|
XP_011526201.1:p.Ala404=
|
|
XM_011527900.2:c.1212C>G
|
XP_011526202.1:p.Ala404=
|
|
XM_017026580.1:c.1212C>G
|
XP_016882069.1:p.Ala404=
|
|
NM_000159.4:c.1212C>G
MANE Select
|
NP_000150.1:p.Ala404=
|
|
NM_013976.4:c.1212C>G
|
NP_039663.1:p.Ala404=
|
|
NM_013976.5:c.1212C>G
|
NP_039663.1:p.Ala404=
|
|