ENST00000029410.10:c.237G>T
MANE Select
|
ENSP00000029410.5:p.Pro79=
|
|
ENST00000029410.9:c.237G>T
|
ENSP00000029410.5:p.Pro79=
|
|
ENST00000502420.1:n.216G>T
|
|
|
ENST00000505433.5:c.237G>T
|
ENSP00000425591.1:p.Pro79=
|
|
ENST00000505468.1:c.-106G>T
|
ENSP00000420886.1:n.-106G>T
|
|
ENST00000507061.1:c.54G>T
|
ENSP00000423868.1:p.Pro18=
|
|
ENST00000510761.1:c.-106G>T
|
ENSP00000423438.1:n.-106G>T
|
|
NM_007255.2:c.237G>T
|
NP_009186.1:p.Pro79=
|
|
XM_005265805.2:c.-106G>T
|
XP_005265862.1:n.-106G>T
|
|
XM_006714816.2:c.-263G>T
|
XP_006714879.1:n.-263G>T
|
|
XM_011534421.1:c.-106G>T
|
XP_011532723.1:n.-106G>T
|
|
XM_006714816.4:c.-263G>T
|
XP_006714879.1:n.-263G>T
|
|
XM_017008999.2:c.-106G>T
|
XP_016864488.1:n.-106G>T
|
|
NM_007255.3:c.237G>T
MANE Select
|
NP_009186.1:p.Pro79=
|
|