ENST00000399503.4:c.806T>C
MANE Select
|
ENSP00000382423.3:p.Val269Ala
|
|
ENST00000399503.3:c.806T>C
|
ENSP00000382423.3:p.Val269Ala
|
|
NM_005921.1:c.806T>C
|
NP_005912.1:p.Val269Ala
|
|
XM_005248519.3:c.428T>C
|
XP_005248576.2:p.Val143Ala
|
|
XM_011543406.1:c.551T>C
|
XP_011541708.1:p.Val184Ala
|
|
XM_011543407.1:c.806T>C
|
XP_011541709.1:p.Val269Ala
|
|
XM_011543408.1:c.806T>C
|
XP_011541710.1:p.Val269Ala
|
|
XM_017009484.1:c.395T>C
|
XP_016864973.1:p.Val132Ala
|
|
XM_017009485.1:c.317T>C
|
XP_016864974.1:p.Val106Ala
|
|
XR_001742068.2:n.837T>C
|
|
|
NM_005921.2:c.806T>C
MANE Select
|
NP_005912.1:p.Val269Ala
|
|