ENST00000029410.10:c.723+39T>C
MANE Select
|
ENSP00000029410.5:n.723+39T>C
|
|
ENST00000029410.9:c.723+39T>C
|
ENSP00000029410.5:n.723+39T>C
|
|
ENST00000505145.1:n.1821+39T>C
|
|
|
ENST00000505433.5:c.*229+39T>C
|
ENSP00000425591.1:n.*229+39T>C
|
|
ENST00000515353.1:n.1297T>C
|
|
|
NM_007255.2:c.723+39T>C
|
NP_009186.1:n.723+39T>C
|
|
XM_005265805.2:c.381+39T>C
|
XP_005265862.1:n.381+39T>C
|
|
XM_006714816.2:c.243+39T>C
|
XP_006714879.1:n.243+39T>C
|
|
XM_011534421.1:c.381+39T>C
|
XP_011532723.1:n.381+39T>C
|
|
XM_006714816.4:c.243+39T>C
|
XP_006714879.1:n.243+39T>C
|
|
XM_017008999.2:c.381+39T>C
|
XP_016864488.1:n.381+39T>C
|
|
NM_007255.3:c.723+39T>C
MANE Select
|
NP_009186.1:n.723+39T>C
|
|