ENST00000399503.4:c.3116C>G
MANE Select
|
ENSP00000382423.3:p.Ser1039Ter
|
|
ENST00000399503.3:c.3116C>G
|
ENSP00000382423.3:p.Ser1039Ter
|
|
NM_005921.1:c.3116C>G
|
NP_005912.1:p.Ser1039Ter
|
|
XM_005248519.3:c.2738C>G
|
XP_005248576.2:p.Ser913Ter
|
|
XM_011543406.1:c.2861C>G
|
XP_011541708.1:p.Ser954Ter
|
|
XM_011543407.1:c.2837C>G
|
XP_011541709.1:p.Ser946Ter
|
|
XM_011543408.1:c.3116C>G
|
XP_011541710.1:p.Ser1039Ter
|
|
XM_017009484.1:c.2705C>G
|
XP_016864973.1:p.Ser902Ter
|
|
XM_017009485.1:c.2627C>G
|
XP_016864974.1:p.Ser876Ter
|
|
XR_001742068.2:n.3147C>G
|
|
|
NM_005921.2:c.3116C>G
MANE Select
|
NP_005912.1:p.Ser1039Ter
|
|