ENST00000597188.6:c.3256T>A
MANE Select
|
ENSP00000471851.1:p.Phe1086Ile
|
|
ENST00000270328.8:c.3256T>A
|
ENSP00000270328.4:p.Phe1086Ile
|
|
ENST00000593913.5:c.*2133T>A
|
ENSP00000469901.1:n.*2133T>A
|
|
ENST00000595838.5:c.1717T>A
|
ENSP00000470501.1:p.Phe573Ile
|
|
ENST00000597188.5:c.3256T>A
|
ENSP00000471851.1:p.Phe1086Ile
|
|
NM_001282352.1:c.1717T>A
|
NP_001269281.1:p.Phe573Ile
|
|
NM_030957.3:c.3256T>A
|
NP_112219.3:p.Phe1086Ile
|
|
XM_006722917.2:c.2299T>A
|
XP_006722980.1:p.Phe767Ile
|
|
XM_011528331.1:c.3403T>A
|
XP_011526633.1:p.Phe1135Ile
|
|
XM_011528332.1:c.3403T>A
|
XP_011526634.1:p.Phe1135Ile
|
|
XM_011528333.1:c.3403T>A
|
XP_011526635.1:p.Phe1135Ile
|
|
XM_011528334.1:c.3079T>A
|
XP_011526636.1:p.Phe1027Ile
|
|
XM_011528335.1:c.1972T>A
|
XP_011526637.1:p.Phe658Ile
|
|
XM_011528336.1:c.1966T>A
|
XP_011526638.1:p.Phe656Ile
|
|
XM_006722917.3:c.2299T>A
|
XP_006722980.1:p.Phe767Ile
|
|
XM_017027338.2:c.3256T>A
|
XP_016882827.1:p.Phe1086Ile
|
|
XM_017027339.1:c.1825T>A
|
XP_016882828.1:p.Phe609Ile
|
|
XM_017027340.1:c.1819T>A
|
XP_016882829.1:p.Phe607Ile
|
|
NM_030957.4:c.3256T>A
MANE Select
|
NP_112219.3:p.Phe1086Ile
|
|
NM_001282352.2:c.1717T>A
|
NP_001269281.1:p.Phe573Ile
|
|