ENST00000651671.1:c.6037G>T
MANE Select
|
ENSP00000498587.1:p.Asp2013Tyr
|
|
ENST00000679595.1:c.*1077G>T
|
ENSP00000506241.1:n.*1077G>T
|
|
ENST00000679969.1:n.2518G>T
|
|
|
ENST00000680003.1:n.2369G>T
|
|
|
ENST00000680133.1:c.5923G>T
|
ENSP00000505319.1:p.Asp1975Tyr
|
|
ENST00000680218.1:c.5917G>T
|
ENSP00000505339.1:p.Asp1973Tyr
|
|
ENST00000680668.1:c.5923G>T
|
ENSP00000506336.1:p.Asp1975Tyr
|
|
ENST00000680778.1:c.3634G>T
|
ENSP00000506033.1:p.Asp1212Tyr
|
|
ENST00000680924.1:c.*3437G>T
|
ENSP00000506031.1:n.*3437G>T
|
|
ENST00000681135.1:c.*3646G>T
|
ENSP00000506636.1:n.*3646G>T
|
|
ENST00000681298.1:n.4142G>T
|
|
|
ENST00000681454.1:c.*5273G>T
|
ENSP00000505763.1:n.*5273G>T
|
|
ENST00000277541.6:c.6037G>T
|
ENSP00000277541.6:p.Asp2013Tyr
|
|
NM_017617.3:c.6037G>T
|
NP_060087.3:p.Asp2013Tyr
|
|
XM_011518717.1:c.5338G>T
|
XP_011517019.1:p.Asp1780Tyr
|
|
NM_017617.5:c.6037G>T
MANE Select
|
NP_060087.3:p.Asp2013Tyr
|
|
XM_011518717.2:c.5314G>T
|
XP_011517019.2:p.Asp1772Tyr
|
|