ENST00000317357.10:c.1908G=
MANE Select
|
ENSP00000318900.5:p.Ala636=
|
|
ENST00000317357.9:c.1908G=
|
ENSP00000318900.5:p.Ala636=
|
|
NM_018013.3:c.1908G=
|
NP_060483.3:p.Ala636=
|
|
XM_005267041.3:c.2061G=
|
XP_005267098.1:p.Ala687=
|
|
XM_005267042.3:c.1965G=
|
XP_005267099.1:p.Ala655=
|
|
XM_011535920.1:c.2061G=
|
XP_011534222.1:p.Ala687=
|
|
XM_011535921.1:c.1947G=
|
XP_011534223.1:p.Ala649=
|
|
XM_011535922.1:c.1320G=
|
XP_011534224.1:p.Ala440=
|
|
XM_011535923.1:c.1131G=
|
XP_011534225.1:p.Ala377=
|
|
XM_005267041.4:c.2061G=
|
XP_005267098.1:p.Ala687=
|
|
XM_005267042.4:c.1965G=
|
XP_005267099.1:p.Ala655=
|
|
XM_011535920.2:c.2061G=
|
XP_011534222.1:p.Ala687=
|
|
XM_011535921.2:c.1947G=
|
XP_011534223.1:p.Ala649=
|
|
XM_011535923.2:c.1131G=
|
XP_011534225.1:p.Ala377=
|
|
XM_017010991.1:c.1461G=
|
XP_016866480.1:p.Ala487=
|
|
XM_017010992.1:c.1461G=
|
XP_016866481.1:p.Ala487=
|
|
XM_017010993.1:c.1461G=
|
XP_016866482.1:p.Ala487=
|
|
XM_017010994.1:c.1461G=
|
XP_016866483.1:p.Ala487=
|
|
NM_018013.4:c.1908G=
MANE Select
|
NP_060483.3:p.Ala636=
|
|