ENST00000222390.11:c.996G>T
MANE Select
|
ENSP00000222390.5:p.Gln332His
|
|
ENST00000457544.7:c.981G>T
|
ENSP00000391238.2:p.Gln327His
|
|
ENST00000222390.9:c.996G>T
|
ENSP00000222390.5:p.Gln332His
|
|
ENST00000457544.6:c.981G>T
|
ENSP00000391238.2:p.Gln327His
|
|
NM_000601.4:c.996G>T
|
NP_000592.3:p.Gln332His
|
|
NM_001010932.1:c.981G>T
|
NP_001010932.1:p.Gln327His
|
|
XM_006715956.2:c.996G>T
|
XP_006716019.1:p.Gln332His
|
|
XM_011516115.1:c.981G>T
|
XP_011514417.1:p.Gln327His
|
|
NM_000601.5:c.996G>T
|
NP_000592.3:p.Gln332His
|
|
NM_001010932.2:c.981G>T
|
NP_001010932.1:p.Gln327His
|
|
XM_011516115.2:c.981G>T
|
XP_011514417.1:p.Gln327His
|
|
NM_000601.6:c.996G>T
MANE Select
|
NP_000592.3:p.Gln332His
|
|
NM_001010932.3:c.981G>T
|
NP_001010932.1:p.Gln327His
|
|