ENST00000399503.4:c.773C>G
MANE Select
|
ENSP00000382423.3:p.Ser258Ter
|
|
ENST00000399503.3:c.773C>G
|
ENSP00000382423.3:p.Ser258Ter
|
|
NM_005921.1:c.773C>G
|
NP_005912.1:p.Ser258Ter
|
|
XM_005248519.3:c.395C>G
|
XP_005248576.2:p.Ser132Ter
|
|
XM_011543406.1:c.518C>G
|
XP_011541708.1:p.Ser173Ter
|
|
XM_011543407.1:c.773C>G
|
XP_011541709.1:p.Ser258Ter
|
|
XM_011543408.1:c.773C>G
|
XP_011541710.1:p.Ser258Ter
|
|
XM_017009484.1:c.362C>G
|
XP_016864973.1:p.Ser121Ter
|
|
XM_017009485.1:c.284C>G
|
XP_016864974.1:p.Ser95Ter
|
|
XR_001742068.2:n.804C>G
|
|
|
NM_005921.2:c.773C>G
MANE Select
|
NP_005912.1:p.Ser258Ter
|
|