ENST00000344327.8:c.1779A>C
MANE Select
|
ENSP00000340913.3:p.Ile593=
|
|
ENST00000344327.7:c.1779A>C
|
ENSP00000340913.3:p.Ile593=
|
|
ENST00000348423.8:c.1431A>C
|
ENSP00000343672.4:p.Ile477=
|
|
ENST00000360497.4:c.1614A>C
|
ENSP00000353687.4:p.Ile538=
|
|
ENST00000532133.5:c.1545A>C
|
ENSP00000435574.1:p.Ile515=
|
|
NM_004621.5:c.1779A>C
|
NP_004612.2:p.Ile593=
|
|
XM_006718898.2:c.1779A>C
|
XP_006718961.1:p.Ile593=
|
|
XM_011542968.1:c.1614A>C
|
XP_011541270.1:p.Ile538=
|
|
XM_011542969.1:c.1779A>C
|
XP_011541271.1:p.Ile593=
|
|
XM_011542968.3:c.1614A>C
|
XP_011541270.1:p.Ile538=
|
|
XM_017018221.2:c.1431A>C
|
XP_016873710.1:p.Ile477=
|
|
XR_001747948.2:n.2135A>C
|
|
|
NM_004621.6:c.1779A>C
MANE Select
|
NP_004612.2:p.Ile593=
|
|