ENST00000398215.3:c.555G>C
MANE Select
|
ENSP00000381273.2:p.Gln185His
|
|
ENST00000651629.1:c.555G>C
|
ENSP00000498905.1:p.Gln185His
|
|
ENST00000398215.2:c.555G>C
|
ENSP00000381273.2:p.Gln185His
|
|
NM_000496.2:c.555G>C
|
NP_000487.1:p.Gln185His
|
|
XM_006724141.2:c.555G>C
|
XP_006724204.1:p.Gln185His
|
|
XM_011529900.1:c.555G>C
|
XP_011528202.1:p.Gln185His
|
|
XM_011529901.1:c.555G>C
|
XP_011528203.1:p.Gln185His
|
|
XM_006724141.3:c.555G>C
|
XP_006724204.1:p.Gln185His
|
|
XM_011529900.2:c.555G>C
|
XP_011528202.1:p.Gln185His
|
|
NM_000496.3:c.555G>C
MANE Select
|
NP_000487.1:p.Gln185His
|
|