ENST00000367069.7:c.791C>T
MANE Select
|
ENSP00000356036.1:p.Ala264Val
|
|
ENST00000252655.1:c.1217C>T
|
ENSP00000252655.1:p.Ala406Val
|
|
ENST00000367069.6:c.791C>T
|
ENSP00000356036.1:p.Ala264Val
|
|
ENST00000449822.5:c.503C>T
|
ENSP00000393195.1:p.Ala168Val
|
|
NM_031924.4:c.1217C>T
|
NP_114130.3:p.Ala406Val
|
|
XM_005267153.3:c.929C>T
|
XP_005267210.1:p.Ala310Val
|
|
XR_245553.2:n.1673C>T
|
|
|
NM_001346418.1:c.929C>T
|
NP_001333347.1:p.Ala310Val
|
|
NM_031924.5:c.1217C>T
|
NP_114130.3:p.Ala406Val
|
|
NR_144434.1:n.1428C>T
|
|
|
XM_017011347.2:c.401C>T
|
XP_016866836.1:p.Ala134Val
|
|
XM_024446566.1:c.401C>T
|
XP_024302334.1:p.Ala134Val
|
|
XR_001743668.2:n.1667C>T
|
|
|
XR_001743669.2:n.1667C>T
|
|
|
XR_001743670.2:n.1379C>T
|
|
|
XR_001743671.2:n.873C>T
|
|
|
NM_031924.6:c.1217C>T
|
NP_114130.3:p.Ala406Val
|
|
NM_031924.8:c.791C>T
MANE Select
|
NP_114130.4:p.Ala264Val
|
|