ENST00000374479.4:c.1074T>G
MANE Select
|
ENSP00000363603.3:p.Val358=
|
|
ENST00000374479.3:c.1074T>G
|
ENSP00000363603.3:p.Val358=
|
|
NM_000147.4:c.1074T>G
|
NP_000138.2:p.Val358=
|
|
XM_005245821.1:c.699T>G
|
XP_005245878.1:p.Val233=
|
|
XM_011541167.1:c.441T>G
|
XP_011539469.1:p.Val147=
|
|
XM_005245821.3:c.699T>G
|
XP_005245878.1:p.Val233=
|
|
XM_011541167.3:c.441T>G
|
XP_011539469.1:p.Val147=
|
|
XM_017000905.2:c.771T>G
|
XP_016856394.1:p.Val257=
|
|
NM_000147.5:c.1074T>G
MANE Select
|
NP_000138.2:p.Val358=
|
|
NR_174379.1:n.1252T>G
|
|
|
NR_174380.1:n.1301T>G
|
|
|
NR_174381.1:n.1140T>G
|
|
|
NR_174382.1:n.1537T>G
|
|
|