ENST00000399503.4:c.3002T>A
MANE Select
|
ENSP00000382423.3:p.Val1001Asp
|
|
ENST00000399503.3:c.3002T>A
|
ENSP00000382423.3:p.Val1001Asp
|
|
NM_005921.1:c.3002T>A
|
NP_005912.1:p.Val1001Asp
|
|
XM_005248519.3:c.2624T>A
|
XP_005248576.2:p.Val875Asp
|
|
XM_011543406.1:c.2747T>A
|
XP_011541708.1:p.Val916Asp
|
|
XM_011543407.1:c.2723T>A
|
XP_011541709.1:p.Val908Asp
|
|
XM_011543408.1:c.3002T>A
|
XP_011541710.1:p.Val1001Asp
|
|
XM_017009484.1:c.2591T>A
|
XP_016864973.1:p.Val864Asp
|
|
XM_017009485.1:c.2513T>A
|
XP_016864974.1:p.Val838Asp
|
|
XR_001742068.2:n.3033T>A
|
|
|
NM_005921.2:c.3002T>A
MANE Select
|
NP_005912.1:p.Val1001Asp
|
|