ENST00000399503.4:c.2945C>A
MANE Select
|
ENSP00000382423.3:p.Ala982Asp
|
|
ENST00000399503.3:c.2945C>A
|
ENSP00000382423.3:p.Ala982Asp
|
|
NM_005921.1:c.2945C>A
|
NP_005912.1:p.Ala982Asp
|
|
XM_005248519.3:c.2567C>A
|
XP_005248576.2:p.Ala856Asp
|
|
XM_011543406.1:c.2690C>A
|
XP_011541708.1:p.Ala897Asp
|
|
XM_011543407.1:c.2666C>A
|
XP_011541709.1:p.Ala889Asp
|
|
XM_011543408.1:c.2945C>A
|
XP_011541710.1:p.Ala982Asp
|
|
XM_017009484.1:c.2534C>A
|
XP_016864973.1:p.Ala845Asp
|
|
XM_017009485.1:c.2456C>A
|
XP_016864974.1:p.Ala819Asp
|
|
XR_001742068.2:n.2976C>A
|
|
|
NM_005921.2:c.2945C>A
MANE Select
|
NP_005912.1:p.Ala982Asp
|
|