ENST00000225573.5:c.534T>C
|
ENSP00000225573.5:p.Gly178=
|
|
ENST00000434554.7:c.609T>C
|
ENSP00000399960.3:p.Gly203=
|
|
ENST00000582171.6:c.*328T>C
|
ENSP00000463994.1:n.*328T>C
|
|
ENST00000583599.6:c.423T>C
|
ENSP00000463919.2:p.Gly141=
|
|
ENST00000584061.6:c.594T>C
|
ENSP00000463972.2:p.Gly198=
|
|
ENST00000584806.2:n.332T>C
|
|
|
ENST00000641285.1:n.443T>C
|
|
|
ENST00000641305.1:n.2162T>C
|
|
|
ENST00000641323.1:c.*682T>C
|
ENSP00000492965.1:n.*682T>C
|
|
ENST00000641427.1:n.663T>C
|
|
|
ENST00000641511.1:c.395T>C
|
|
|
ENST00000641703.1:c.379T>C
|
ENSP00000493219.1:n.379T>C
|
|
ENST00000641709.1:c.*485T>C
|
ENSP00000493349.1:n.*485T>C
|
|
ENST00000641856.1:c.*1171T>C
|
ENSP00000493224.1:n.*1171T>C
|
|
ENST00000642017.2:c.663T>C
MANE Select
|
ENSP00000493302.2:p.Gly221=
|
|
ENST00000225573.4:c.663T>C
|
ENSP00000225573.4:p.Gly221=
|
|
ENST00000434554.6:c.534T>C
|
ENSP00000399960.2:p.Gly178=
|
|
ENST00000582171.5:c.*328T>C
|
ENSP00000463994.1:n.*328T>C
|
|
ENST00000584806.1:n.332T>C
|
|
|
ENST00000585320.5:c.*145T>C
|
ENSP00000462345.1:n.*145T>C
|
|
NM_018129.3:c.663T>C
|
NP_060599.1:p.Gly221=
|
|
XM_005257500.2:c.423T>C
|
XP_005257557.1:p.Gly141=
|
|
XM_011524968.1:c.378T>C
|
XP_011523270.1:p.Gly126=
|
|
XM_005257500.3:c.423T>C
|
XP_005257557.1:p.Gly141=
|
|
XM_011524968.2:c.378T>C
|
XP_011523270.1:p.Gly126=
|
|
XM_017024813.1:c.423T>C
|
XP_016880302.1:p.Gly141=
|
|
NM_018129.4:c.663T>C
MANE Select
|
NP_060599.1:p.Gly221=
|
|