ENST00000597188.6:c.940T>A
MANE Select
|
ENSP00000471851.1:p.Phe314Ile
|
|
ENST00000270328.8:c.940T>A
|
ENSP00000270328.4:p.Phe314Ile
|
|
ENST00000593913.5:c.*75T>A
|
ENSP00000469901.1:n.*75T>A
|
|
ENST00000596851.5:c.*75T>A
|
ENSP00000469559.1:n.*75T>A
|
|
ENST00000597188.5:c.940T>A
|
ENSP00000471851.1:p.Phe314Ile
|
|
ENST00000601163.1:n.135T>A
|
|
|
NM_030957.3:c.940T>A
|
NP_112219.3:p.Phe314Ile
|
|
XM_006722917.2:c.-165T>A
|
XP_006722980.1:n.-165T>A
|
|
XM_011528331.1:c.940T>A
|
XP_011526633.1:p.Phe314Ile
|
|
XM_011528332.1:c.940T>A
|
XP_011526634.1:p.Phe314Ile
|
|
XM_011528333.1:c.940T>A
|
XP_011526635.1:p.Phe314Ile
|
|
XM_011528334.1:c.940T>A
|
XP_011526636.1:p.Phe314Ile
|
|
XR_430156.2:n.1216T>A
|
|
|
XR_936208.1:n.1216T>A
|
|
|
XR_936209.1:n.1216T>A
|
|
|
XM_006722917.3:c.-165T>A
|
XP_006722980.1:n.-165T>A
|
|
XM_017027338.2:c.940T>A
|
XP_016882827.1:p.Phe314Ile
|
|
XR_001753770.1:n.1776T>A
|
|
|
NM_030957.4:c.940T>A
MANE Select
|
NP_112219.3:p.Phe314Ile
|
|