ENST00000302850.10:c.3094G>C
MANE Select
|
ENSP00000303830.4:p.Gly1032Arg
|
|
ENST00000302850.9:c.3094G>C
|
ENSP00000303830.4:p.Gly1032Arg
|
|
ENST00000341500.9:c.3058G>C
|
ENSP00000342838.4:p.Gly1020Arg
|
|
NM_000208.2:c.3094G>C
|
NP_000199.2:p.Gly1032Arg
|
|
NM_000208.3:c.3094G>C
|
NP_000199.2:p.Gly1032Arg
|
|
NM_001079817.1:c.3058G>C
|
NP_001073285.1:p.Gly1020Arg
|
|
NM_001079817.2:c.3058G>C
|
NP_001073285.1:p.Gly1020Arg
|
|
XM_011527988.1:c.3169G>C
|
XP_011526290.1:p.Gly1057Arg
|
|
XM_011527989.1:c.3133G>C
|
XP_011526291.1:p.Gly1045Arg
|
|
XM_011527988.2:c.3091G>C
|
XP_011526290.2:p.Gly1031Arg
|
|
XM_011527989.3:c.3055G>C
|
XP_011526291.2:p.Gly1019Arg
|
|
NM_000208.4:c.3094G>C
MANE Select
|
NP_000199.2:p.Gly1032Arg
|
|
NM_001079817.3:c.3058G>C
|
NP_001073285.1:p.Gly1020Arg
|
|