ENST00000399503.4:c.2573C>T
MANE Select
|
ENSP00000382423.3:p.Ala858Val
|
|
ENST00000399503.3:c.2573C>T
|
ENSP00000382423.3:p.Ala858Val
|
|
NM_005921.1:c.2573C>T
|
NP_005912.1:p.Ala858Val
|
|
XM_005248519.3:c.2195C>T
|
XP_005248576.2:p.Ala732Val
|
|
XM_011543406.1:c.2318C>T
|
XP_011541708.1:p.Ala773Val
|
|
XM_011543407.1:c.2294C>T
|
XP_011541709.1:p.Ala765Val
|
|
XM_011543408.1:c.2573C>T
|
XP_011541710.1:p.Ala858Val
|
|
XM_017009484.1:c.2162C>T
|
XP_016864973.1:p.Ala721Val
|
|
XM_017009485.1:c.2084C>T
|
XP_016864974.1:p.Ala695Val
|
|
XR_001742068.2:n.2604C>T
|
|
|
NM_005921.2:c.2573C>T
MANE Select
|
NP_005912.1:p.Ala858Val
|
|