ENST00000262493.12:c.752T>A
MANE Select
|
ENSP00000262493.6:p.Phe251Tyr
|
|
ENST00000562316.6:c.419T>A
|
ENSP00000457238.2:p.Phe140Tyr
|
|
ENST00000564727.2:c.56T>A
|
ENSP00000454971.2:p.Phe19Tyr
|
|
ENST00000568375.2:c.116-3454T>A
|
|
|
ENST00000638185.1:n.967T>A
|
|
|
ENST00000638210.1:n.1052T>A
|
|
|
ENST00000638705.1:c.752T>A
|
ENSP00000491223.1:p.Phe251Tyr
|
|
ENST00000638836.1:n.662T>A
|
|
|
ENST00000639055.1:n.1473T>A
|
|
|
ENST00000639251.1:n.653T>A
|
|
|
ENST00000639268.1:c.387T>A
|
|
|
ENST00000639341.1:c.277T>A
|
|
|
ENST00000639770.1:c.790T>A
|
ENSP00000491999.1:n.790T>A
|
|
ENST00000640390.1:n.682T>A
|
|
|
ENST00000640469.1:c.116T>A
|
ENSP00000491875.1:p.Phe39Tyr
|
|
ENST00000640560.1:n.528T>A
|
|
|
ENST00000640893.1:c.*150T>A
|
ENSP00000492677.1:n.*150T>A
|
|
ENST00000262493.10:c.752T>A
|
ENSP00000262493.6:p.Phe251Tyr
|
|
ENST00000568375.1:n.116-3454T>A
|
|
|
NM_020988.2:c.752T>A
|
NP_066268.1:p.Phe251Tyr
|
|
XM_011523003.1:c.626T>A
|
XP_011521305.1:p.Phe209Tyr
|
|
XM_011523003.3:c.626T>A
|
XP_011521305.1:p.Phe209Tyr
|
|
NM_020988.3:c.752T>A
MANE Select
|
NP_066268.1:p.Phe251Tyr
|
|