ENST00000029410.10:c.272G=
MANE Select
|
ENSP00000029410.5:p.Gly91=
|
|
ENST00000029410.9:c.272G=
|
ENSP00000029410.5:p.Gly91=
|
|
ENST00000502420.1:n.251G=
|
|
|
ENST00000505433.5:c.272G=
|
ENSP00000425591.1:p.Gly91=
|
|
ENST00000505468.1:c.-71G=
|
ENSP00000420886.1:n.-71G=
|
|
ENST00000507061.1:c.89G=
|
ENSP00000423868.1:p.Gly30=
|
|
ENST00000510761.1:c.-71G=
|
ENSP00000423438.1:n.-71G=
|
|
NM_007255.2:c.272G=
|
NP_009186.1:p.Gly91=
|
|
XM_005265805.2:c.-71G=
|
XP_005265862.1:n.-71G=
|
|
XM_006714816.2:c.-228G=
|
XP_006714879.1:n.-228G=
|
|
XM_011534421.1:c.-71G=
|
XP_011532723.1:n.-71G=
|
|
XM_006714816.4:c.-228G=
|
XP_006714879.1:n.-228G=
|
|
XM_017008999.2:c.-71G=
|
XP_016864488.1:n.-71G=
|
|
NM_007255.3:c.272G=
MANE Select
|
NP_009186.1:p.Gly91=
|
|