ENST00000262418.12:c.1939G>C
MANE Select
|
ENSP00000262418.6:p.Gly647Arg
|
|
ENST00000262418.10:c.1939G>C
|
ENSP00000262418.6:p.Gly647Arg
|
|
ENST00000399246.3:c.841G>C
|
ENSP00000382190.3:p.Gly281Arg
|
|
NM_000342.3:c.1939G>C
|
NP_000333.1:p.Gly647Arg
|
|
XM_005257593.3:c.1744G>C
|
XP_005257650.1:p.Gly582Arg
|
|
XM_011525129.1:c.1849G>C
|
XP_011523431.1:p.Gly617Arg
|
|
XM_011525130.1:c.1939G>C
|
XP_011523432.1:p.Gly647Arg
|
|
XM_011525131.1:c.1939G>C
|
XP_011523433.1:p.Gly647Arg
|
|
XM_005257593.5:c.1744G>C
|
XP_005257650.1:p.Gly582Arg
|
|
XM_011525129.2:c.1849G>C
|
XP_011523431.1:p.Gly617Arg
|
|
NM_000342.4:c.1939G>C
MANE Select
|
NP_000333.1:p.Gly647Arg
|
|