ENST00000355773.6:c.1294T>A
MANE Select
|
ENSP00000348019.5:p.Phe432Ile
|
|
ENST00000355773.5:c.1294T>A
|
ENSP00000348019.5:p.Phe432Ile
|
|
NM_012434.4:c.1294T>A
|
NP_036566.1:p.Phe432Ile
|
|
XM_005248710.2:c.1243T>A
|
XP_005248767.1:p.Phe415Ile
|
|
XM_005248711.1:c.1096T>A
|
XP_005248768.1:p.Phe366Ile
|
|
XM_011535750.1:c.1146T>A
|
XP_011534052.1:p.His382Gln
|
|
NM_012434.5:c.1294T>A
MANE Select
|
NP_036566.1:p.Phe432Ile
|
|
NM_001382629.1:c.1063T>A
|
NP_001369558.1:p.Phe355Ile
|
|
NM_001382630.1:c.1260-5193T>A
|
NP_001369559.1:n.1260-5193T>A
|
|
NM_001382631.1:c.1315T>A
|
NP_001369560.1:p.Phe439Ile
|
|
NM_001382632.1:c.1207T>A
|
NP_001369561.1:p.Phe403Ile
|
|
NM_001382633.1:c.1294T>A
|
NP_001369562.1:p.Phe432Ile
|
|
NM_001382634.1:c.1135T>A
|
NP_001369563.1:p.Phe379Ile
|
|
NM_001382635.1:c.1291T>A
|
NP_001369564.1:p.Phe431Ile
|
|
NM_001382636.1:c.976T>A
|
NP_001369565.1:p.Phe326Ile
|
|