ENST00000401061.9:c.327C>A
MANE Select
|
ENSP00000383840.4:p.Pro109=
|
|
ENST00000401061.8:c.327C>A
|
ENSP00000383840.4:p.Pro109=
|
|
ENST00000616135.1:c.156C>A
|
ENSP00000478859.1:p.Pro52=
|
|
NM_015506.2:c.327C>A
|
NP_056321.2:p.Pro109=
|
|
XM_005270724.3:c.132C>A
|
XP_005270781.1:p.Pro44=
|
|
XM_011541204.1:c.156C>A
|
XP_011539506.1:p.Pro52=
|
|
NM_001330540.1:c.156C>A
|
NP_001317469.1:p.Pro52=
|
|
XM_005270724.5:c.132C>A
|
XP_005270781.1:p.Pro44=
|
|
NM_015506.3:c.327C>A
MANE Select
|
NP_056321.2:p.Pro109=
|
|
NM_001330540.2:c.156C>A
|
NP_001317469.1:p.Pro52=
|
|