ENST00000373631.8:c.3660C>T
MANE Select
|
ENSP00000362734.3:p.Phe1220=
|
|
ENST00000373631.7:c.3660C>T
|
ENSP00000362734.3:p.Phe1220=
|
|
ENST00000460253.1:c.2664C>T
|
ENSP00000435279.1:p.Phe888=
|
|
NM_173689.6:c.3660C>T
|
NP_775960.4:p.Phe1220=
|
|
NR_104603.1:n.2774C>T
|
|
|
XM_005251934.1:c.2664C>T
|
XP_005251991.1:p.Phe888=
|
|
XM_011518556.1:c.3633C>T
|
XP_011516858.1:p.Phe1211=
|
|
XM_011518557.1:c.3465C>T
|
XP_011516859.1:p.Phe1155=
|
|
XM_011518558.1:c.3465C>T
|
XP_011516860.1:p.Phe1155=
|
|
XM_005251934.3:c.2664C>T
|
XP_005251991.1:p.Phe888=
|
|
XM_011518556.3:c.3633C>T
|
XP_011516858.1:p.Phe1211=
|
|
XM_011518557.3:c.3465C>T
|
XP_011516859.1:p.Phe1155=
|
|
XM_011518558.3:c.3465C>T
|
XP_011516860.1:p.Phe1155=
|
|
NM_173689.7:c.3660C>T
MANE Select
|
NP_775960.4:p.Phe1220=
|
|
NR_104603.2:n.2774C>T
|
|
|