ENST00000449082.3:c.3138G>C
MANE Select
|
ENSP00000390600.2:p.Arg1046Ser
|
|
ENST00000643924.1:c.3135G>C
|
ENSP00000495595.1:p.Arg1045Ser
|
|
ENST00000655275.1:c.3162G>C
|
ENSP00000499510.1:p.Arg1054Ser
|
|
ENST00000449082.2:c.3138G>C
|
ENSP00000390600.2:p.Arg1046Ser
|
|
NM_001293306.2:c.3135G>C
|
NP_001280235.2:p.Arg1045Ser
|
|
NM_001293307.2:c.2844G>C
|
NP_001280236.2:p.Arg948Ser
|
|
NM_006514.3:c.3138G>C
|
NP_006505.3:p.Arg1046Ser
|
|
XM_005265371.2:c.3147G>C
|
XP_005265428.1:p.Arg1049Ser
|
|
XM_011533993.1:c.3144G>C
|
XP_011532295.1:p.Arg1048Ser
|
|
XM_011533994.1:c.2853G>C
|
XP_011532296.1:p.Arg951Ser
|
|
XM_005265371.3:c.3147G>C
|
XP_005265428.1:p.Arg1049Ser
|
|
XM_011533993.2:c.3144G>C
|
XP_011532295.1:p.Arg1048Ser
|
|
XM_011533994.2:c.2853G>C
|
XP_011532296.1:p.Arg951Ser
|
|
NM_006514.4:c.3138G>C
MANE Select
|
NP_006505.4:p.Arg1046Ser
|
|