ENST00000449082.3:c.3202G>C
MANE Select
|
ENSP00000390600.2:p.Glu1068Gln
|
|
ENST00000643924.1:c.3199G>C
|
ENSP00000495595.1:p.Glu1067Gln
|
|
ENST00000655275.1:c.3226G>C
|
ENSP00000499510.1:p.Glu1076Gln
|
|
ENST00000449082.2:c.3202G>C
|
ENSP00000390600.2:p.Glu1068Gln
|
|
NM_001293306.2:c.3199G>C
|
NP_001280235.2:p.Glu1067Gln
|
|
NM_001293307.2:c.2908G>C
|
NP_001280236.2:p.Glu970Gln
|
|
NM_006514.3:c.3202G>C
|
NP_006505.3:p.Glu1068Gln
|
|
XM_005265371.2:c.3211G>C
|
XP_005265428.1:p.Glu1071Gln
|
|
XM_011533993.1:c.3208G>C
|
XP_011532295.1:p.Glu1070Gln
|
|
XM_011533994.1:c.2917G>C
|
XP_011532296.1:p.Glu973Gln
|
|
XM_005265371.3:c.3211G>C
|
XP_005265428.1:p.Glu1071Gln
|
|
XM_011533993.2:c.3208G>C
|
XP_011532295.1:p.Glu1070Gln
|
|
XM_011533994.2:c.2917G>C
|
XP_011532296.1:p.Glu973Gln
|
|
NM_006514.4:c.3202G>C
MANE Select
|
NP_006505.4:p.Glu1068Gln
|
|