ENST00000248633.9:c.2598T>C
MANE Select
|
ENSP00000248633.4:p.Phe866=
|
|
ENST00000248633.8:c.2598T>C
|
ENSP00000248633.4:p.Phe866=
|
|
ENST00000428214.5:c.2427T>C
|
ENSP00000394413.1:p.Phe809=
|
|
ENST00000438045.5:c.1632T>C
|
ENSP00000410438.1:p.Phe544=
|
|
ENST00000484913.5:n.2637T>C
|
|
|
ENST00000496420.5:n.2490T>C
|
|
|
NM_000466.2:c.2598T>C
|
NP_000457.1:p.Phe866=
|
|
NM_001282677.1:c.2427T>C
|
NP_001269606.1:p.Phe809=
|
|
NM_001282678.1:c.1974T>C
|
NP_001269607.1:p.Phe658=
|
|
XM_005250433.3:c.849T>C
|
XP_005250490.1:p.Phe283=
|
|
XR_242246.3:n.2694T>C
|
|
|
XM_017012319.2:c.849T>C
|
XP_016867808.1:p.Phe283=
|
|
XR_001744808.2:n.1625T>C
|
|
|
XR_242246.5:n.2645T>C
|
|
|
NM_000466.3:c.2598T>C
MANE Select
|
NP_000457.1:p.Phe866=
|
|
NM_001282677.2:c.2427T>C
|
NP_001269606.1:p.Phe809=
|
|
NM_001282678.2:c.1974T>C
|
NP_001269607.1:p.Phe658=
|
|