ENST00000651671.1:c.6503G>A
MANE Select
|
ENSP00000498587.1:p.Cys2168Tyr
|
|
ENST00000679595.1:c.*1543G>A
|
ENSP00000506241.1:n.*1543G>A
|
|
ENST00000679969.1:n.3099G>A
|
|
|
ENST00000680003.1:n.2835G>A
|
|
|
ENST00000680133.1:c.6389G>A
|
ENSP00000505319.1:p.Cys2130Tyr
|
|
ENST00000680218.1:c.6383G>A
|
ENSP00000505339.1:p.Cys2128Tyr
|
|
ENST00000680668.1:c.6389G>A
|
ENSP00000506336.1:p.Cys2130Tyr
|
|
ENST00000680778.1:c.4100G>A
|
ENSP00000506033.1:p.Cys1367Tyr
|
|
ENST00000680924.1:c.*3903G>A
|
ENSP00000506031.1:n.*3903G>A
|
|
ENST00000681135.1:c.*4112G>A
|
ENSP00000506636.1:n.*4112G>A
|
|
ENST00000681298.1:n.4608G>A
|
|
|
ENST00000681454.1:c.*5739G>A
|
ENSP00000505763.1:n.*5739G>A
|
|
ENST00000277541.6:c.6503G>A
|
ENSP00000277541.6:p.Cys2168Tyr
|
|
NM_017617.3:c.6503G>A
|
NP_060087.3:p.Cys2168Tyr
|
|
XM_011518717.1:c.5804G>A
|
XP_011517019.1:p.Cys1935Tyr
|
|
NM_017617.5:c.6503G>A
MANE Select
|
NP_060087.3:p.Cys2168Tyr
|
|
XM_011518717.2:c.5780G>A
|
XP_011517019.2:p.Cys1927Tyr
|
|