ENST00000399503.4:c.696T>G
MANE Select
|
ENSP00000382423.3:p.Ser232=
|
|
ENST00000399503.3:c.696T>G
|
ENSP00000382423.3:p.Ser232=
|
|
NM_005921.1:c.696T>G
|
NP_005912.1:p.Ser232=
|
|
XM_005248519.3:c.318T>G
|
XP_005248576.2:p.Ser106=
|
|
XM_011543406.1:c.441T>G
|
XP_011541708.1:p.Ser147=
|
|
XM_011543407.1:c.696T>G
|
XP_011541709.1:p.Ser232=
|
|
XM_011543408.1:c.696T>G
|
XP_011541710.1:p.Ser232=
|
|
XM_017009484.1:c.285T>G
|
XP_016864973.1:p.Ser95=
|
|
XM_017009485.1:c.207T>G
|
XP_016864974.1:p.Ser69=
|
|
XR_001742068.2:n.727T>G
|
|
|
NM_005921.2:c.696T>G
MANE Select
|
NP_005912.1:p.Ser232=
|
|