ENST00000399503.4:c.2694G>C
MANE Select
|
ENSP00000382423.3:p.Glu898Asp
|
|
ENST00000399503.3:c.2694G>C
|
ENSP00000382423.3:p.Glu898Asp
|
|
NM_005921.1:c.2694G>C
|
NP_005912.1:p.Glu898Asp
|
|
XM_005248519.3:c.2316G>C
|
XP_005248576.2:p.Glu772Asp
|
|
XM_011543406.1:c.2439G>C
|
XP_011541708.1:p.Glu813Asp
|
|
XM_011543407.1:c.2415G>C
|
XP_011541709.1:p.Glu805Asp
|
|
XM_011543408.1:c.2694G>C
|
XP_011541710.1:p.Glu898Asp
|
|
XM_017009484.1:c.2283G>C
|
XP_016864973.1:p.Glu761Asp
|
|
XM_017009485.1:c.2205G>C
|
XP_016864974.1:p.Glu735Asp
|
|
XR_001742068.2:n.2725G>C
|
|
|
NM_005921.2:c.2694G>C
MANE Select
|
NP_005912.1:p.Glu898Asp
|
|