ENST00000229179.9:c.469G>T
MANE Select
|
ENSP00000229179.4:p.Asp157Tyr
|
|
ENST00000229179.8:c.469G>T
|
ENSP00000229179.4:p.Asp157Tyr
|
|
ENST00000378905.6:c.16G>T
|
ENSP00000368185.2:p.Asp6Tyr
|
|
ENST00000535333.5:n.523-12G>T
|
|
|
ENST00000535718.5:c.*12G>T
|
ENSP00000445567.1:n.*12G>T
|
|
ENST00000537598.5:n.535G>T
|
|
|
ENST00000538549.1:c.169G>T
|
ENSP00000440116.1:p.Asp57Tyr
|
|
ENST00000539906.5:c.382G>T
|
ENSP00000441448.1:p.Asp128Tyr
|
|
ENST00000545140.1:n.445G>T
|
|
|
NM_020401.2:c.469G>T
|
NP_065134.1:p.Asp157Tyr
|
|
XM_005269037.2:c.469G>T
|
XP_005269094.1:p.Asp157Tyr
|
|
XM_011538576.1:c.382G>T
|
XP_011536878.1:p.Asp128Tyr
|
|
NM_001330192.1:c.382G>T
|
NP_001317121.1:p.Asp128Tyr
|
|
NM_020401.3:c.469G>T
|
NP_065134.1:p.Asp157Tyr
|
|
XM_005269037.4:c.469G>T
|
XP_005269094.1:p.Asp157Tyr
|
|
NM_020401.4:c.469G>T
MANE Select
|
NP_065134.1:p.Asp157Tyr
|
|
NM_001330192.2:c.382G>T
|
NP_001317121.1:p.Asp128Tyr
|
|