|
NM_017617.5:c.4849T>A
MANE Select
|
NP_060087.3:p.Phe1617Ile
|
|
ENST00000651671.1:c.4849T>A
MANE Select
|
ENSP00000498587.1:p.Phe1617Ile
|
|
NM_017617.3:c.4849T>A
|
NP_060087.3:p.Phe1617Ile
|
|
ENST00000277541.6:c.4849T>A
|
ENSP00000277541.6:p.Phe1617Ile
|
|
ENST00000494783.1:n.4T>A
|
|
|
ENST00000645828.1:n.2656T>A
|
|
|
ENST00000679595.1:c.4849T>A
|
ENSP00000506241.1:p.Phe1617Ile
|
|
ENST00000680133.1:c.4735T>A
|
ENSP00000505319.1:p.Phe1579Ile
|
|
ENST00000680218.1:c.4729T>A
|
ENSP00000505339.1:p.Phe1577Ile
|
|
ENST00000680668.1:c.4735T>A
|
ENSP00000506336.1:p.Phe1579Ile
|
|
ENST00000680778.1:c.2446T>A
|
ENSP00000506033.1:p.Phe816Ile
|
|
ENST00000680924.1:c.*2249T>A
|
ENSP00000506031.1:n.*2249T>A
|
|
ENST00000681135.1:c.*2458T>A
|
ENSP00000506636.1:n.*2458T>A
|
|
ENST00000681298.1:n.1662T>A
|
|
|
ENST00000681454.1:c.*4085T>A
|
ENSP00000505763.1:n.*4085T>A
|
|
XM_011518717.1:c.4150T>A
|
XP_011517019.1:p.Phe1384Ile
|
|
XM_011518717.2:c.4126T>A
|
XP_011517019.2:p.Phe1376Ile
|
