ENST00000298139.7:c.4292T>A
MANE Select
|
ENSP00000298139.5:p.Phe1431Tyr
|
|
ENST00000650667.1:c.*3906T>A
|
ENSP00000498593.1:n.*3906T>A
|
|
ENST00000651946.1:n.516T>A
|
|
|
ENST00000298139.5:c.4292T>A
|
ENSP00000298139.5:p.Phe1431Tyr
|
|
ENST00000521620.5:n.2925T>A
|
|
|
NM_000553.4:c.4292T>A , LRG_524t1:c.4292T>A
|
NP_000544.2:p.Phe1431Tyr
|
|
XM_011544639.1:c.4211T>A
|
XP_011542941.1:p.Phe1404Tyr
|
|
XM_011544640.1:c.2693T>A
|
XP_011542942.1:p.Phe898Tyr
|
|
XR_949643.1:n.88-1777A>T
|
|
|
XR_949644.1:n.88-1777A>T
|
|
|
XR_949645.1:n.88-1777A>T
|
|
|
XR_949646.1:n.88-1777A>T
|
|
|
XR_949647.1:n.701-1777A>T
|
|
|
XR_949648.1:n.603-1777A>T
|
|
|
NM_000553.5:c.4292T>A
|
NP_000544.2:p.Phe1431Tyr
|
|
XM_011544639.3:c.4211T>A
|
XP_011542941.1:p.Phe1404Tyr
|
|
XM_024447265.1:c.4082T>A
|
XP_024303033.1:p.Phe1361Tyr
|
|
NM_000553.6:c.4292T>A
MANE Select
|
NP_000544.2:p.Phe1431Tyr
|
|