ENST00000399503.4:c.2581G>T
MANE Select
|
ENSP00000382423.3:p.Asp861Tyr
|
|
ENST00000399503.3:c.2581G>T
|
ENSP00000382423.3:p.Asp861Tyr
|
|
NM_005921.1:c.2581G>T
|
NP_005912.1:p.Asp861Tyr
|
|
XM_005248519.3:c.2203G>T
|
XP_005248576.2:p.Asp735Tyr
|
|
XM_011543406.1:c.2326G>T
|
XP_011541708.1:p.Asp776Tyr
|
|
XM_011543407.1:c.2302G>T
|
XP_011541709.1:p.Asp768Tyr
|
|
XM_011543408.1:c.2581G>T
|
XP_011541710.1:p.Asp861Tyr
|
|
XM_017009484.1:c.2170G>T
|
XP_016864973.1:p.Asp724Tyr
|
|
XM_017009485.1:c.2092G>T
|
XP_016864974.1:p.Asp698Tyr
|
|
XR_001742068.2:n.2612G>T
|
|
|
NM_005921.2:c.2581G>T
MANE Select
|
NP_005912.1:p.Asp861Tyr
|
|