ENST00000367049.9:c.6462T>C
MANE Select
|
ENSP00000356016.4:p.Pro2154=
|
|
ENST00000367051.6:c.5112T>C
|
ENSP00000356018.1:p.Pro1704=
|
|
ENST00000367052.6:c.5112T>C
|
ENSP00000356019.1:p.Pro1704=
|
|
ENST00000367053.6:c.5112T>C
|
ENSP00000356020.1:p.Pro1704=
|
|
ENST00000400960.7:c.5112T>C
|
ENSP00000383744.2:p.Pro1704=
|
|
ENST00000367049.8:c.6462T>C
|
ENSP00000356016.4:p.Pro2154=
|
|
ENST00000367051.5:c.5112T>C
|
ENSP00000356018.1:p.Pro1704=
|
|
ENST00000367052.5:c.5112T>C
|
ENSP00000356019.1:p.Pro1704=
|
|
ENST00000367053.5:c.5112T>C
|
ENSP00000356020.1:p.Pro1704=
|
|
ENST00000400960.6:c.5112T>C
|
ENSP00000383744.2:p.Pro1704=
|
|
ENST00000529814.1:c.1180-4732T>C
|
|
|
NM_000573.3:c.5112T>C
|
NP_000564.2:p.Pro1704=
|
|
NM_000651.4:c.6462T>C
|
NP_000642.3:p.Pro2154=
|
|
XM_006711166.2:c.6477T>C
|
XP_006711229.1:p.Pro2159=
|
|
XM_011509205.1:c.6477T>C
|
XP_011507507.1:p.Pro2159=
|
|
NM_000651.5:c.6462T>C
|
NP_000642.3:p.Pro2154=
|
|
XM_024453287.1:c.5127T>C
|
XP_024309055.1:p.Pro1709=
|
|
NM_000573.4:c.5112T>C
|
NP_000564.2:p.Pro1704=
|
|
NM_000651.6:c.6462T>C
MANE Select
|
NP_000642.3:p.Pro2154=
|
|