ENST00000399503.4:c.3035G>A
MANE Select
|
ENSP00000382423.3:p.Cys1012Tyr
|
|
ENST00000399503.3:c.3035G>A
|
ENSP00000382423.3:p.Cys1012Tyr
|
|
NM_005921.1:c.3035G>A
|
NP_005912.1:p.Cys1012Tyr
|
|
XM_005248519.3:c.2657G>A
|
XP_005248576.2:p.Cys886Tyr
|
|
XM_011543406.1:c.2780G>A
|
XP_011541708.1:p.Cys927Tyr
|
|
XM_011543407.1:c.2756G>A
|
XP_011541709.1:p.Cys919Tyr
|
|
XM_011543408.1:c.3035G>A
|
XP_011541710.1:p.Cys1012Tyr
|
|
XM_017009484.1:c.2624G>A
|
XP_016864973.1:p.Cys875Tyr
|
|
XM_017009485.1:c.2546G>A
|
XP_016864974.1:p.Cys849Tyr
|
|
XR_001742068.2:n.3066G>A
|
|
|
NM_005921.2:c.3035G>A
MANE Select
|
NP_005912.1:p.Cys1012Tyr
|
|