ENST00000449082.3:c.3114G>T
MANE Select
|
ENSP00000390600.2:p.Arg1038Ser
|
|
ENST00000643924.1:c.3111G>T
|
ENSP00000495595.1:p.Arg1037Ser
|
|
ENST00000655275.1:c.3138G>T
|
ENSP00000499510.1:p.Arg1046Ser
|
|
ENST00000449082.2:c.3114G>T
|
ENSP00000390600.2:p.Arg1038Ser
|
|
NM_001293306.2:c.3111G>T
|
NP_001280235.2:p.Arg1037Ser
|
|
NM_001293307.2:c.2820G>T
|
NP_001280236.2:p.Arg940Ser
|
|
NM_006514.3:c.3114G>T
|
NP_006505.3:p.Arg1038Ser
|
|
XM_005265371.2:c.3123G>T
|
XP_005265428.1:p.Arg1041Ser
|
|
XM_011533993.1:c.3120G>T
|
XP_011532295.1:p.Arg1040Ser
|
|
XM_011533994.1:c.2829G>T
|
XP_011532296.1:p.Arg943Ser
|
|
XM_005265371.3:c.3123G>T
|
XP_005265428.1:p.Arg1041Ser
|
|
XM_011533993.2:c.3120G>T
|
XP_011532295.1:p.Arg1040Ser
|
|
XM_011533994.2:c.2829G>T
|
XP_011532296.1:p.Arg943Ser
|
|
NM_006514.4:c.3114G>T
MANE Select
|
NP_006505.4:p.Arg1038Ser
|
|