ENST00000399503.4:c.3050C>T
MANE Select
|
ENSP00000382423.3:p.Ala1017Val
|
|
ENST00000399503.3:c.3050C>T
|
ENSP00000382423.3:p.Ala1017Val
|
|
NM_005921.1:c.3050C>T
|
NP_005912.1:p.Ala1017Val
|
|
XM_005248519.3:c.2672C>T
|
XP_005248576.2:p.Ala891Val
|
|
XM_011543406.1:c.2795C>T
|
XP_011541708.1:p.Ala932Val
|
|
XM_011543407.1:c.2771C>T
|
XP_011541709.1:p.Ala924Val
|
|
XM_011543408.1:c.3050C>T
|
XP_011541710.1:p.Ala1017Val
|
|
XM_017009484.1:c.2639C>T
|
XP_016864973.1:p.Ala880Val
|
|
XM_017009485.1:c.2561C>T
|
XP_016864974.1:p.Ala854Val
|
|
XR_001742068.2:n.3081C>T
|
|
|
NM_005921.2:c.3050C>T
MANE Select
|
NP_005912.1:p.Ala1017Val
|
|