|
NM_005921.2:c.2416G=
MANE Select
|
NP_005912.1:p.Asp806=
|
|
ENST00000399503.4:c.2416G=
MANE Select
|
ENSP00000382423.3:p.Asp806=
|
|
NM_005921.1:c.2416G=
|
NP_005912.1:p.Asp806=
|
|
ENST00000399503.3:c.2416G=
|
ENSP00000382423.3:p.Asp806=
|
|
XM_005248519.3:c.2038G=
|
XP_005248576.2:p.Asp680=
|
|
XM_011543406.1:c.2161G=
|
XP_011541708.1:p.Asp721=
|
|
XM_011543407.1:c.2137G=
|
XP_011541709.1:p.Asp713=
|
|
XM_011543408.1:c.2416G=
|
XP_011541710.1:p.Asp806=
|
|
XM_017009484.1:c.2005G=
|
XP_016864973.1:p.Asp669=
|
|
XM_017009485.1:c.1927G=
|
XP_016864974.1:p.Asp643=
|
|
XR_001742068.2:n.2447G=
|
|