ENST00000449082.3:c.3103C>T
MANE Select
|
ENSP00000390600.2:p.Gln1035Ter
|
|
ENST00000643924.1:c.3100C>T
|
ENSP00000495595.1:p.Gln1034Ter
|
|
ENST00000655275.1:c.3127C>T
|
ENSP00000499510.1:p.Gln1043Ter
|
|
ENST00000449082.2:c.3103C>T
|
ENSP00000390600.2:p.Gln1035Ter
|
|
NM_001293306.2:c.3100C>T
|
NP_001280235.2:p.Gln1034Ter
|
|
NM_001293307.2:c.2809C>T
|
NP_001280236.2:p.Gln937Ter
|
|
NM_006514.3:c.3103C>T
|
NP_006505.3:p.Gln1035Ter
|
|
XM_005265371.2:c.3112C>T
|
XP_005265428.1:p.Gln1038Ter
|
|
XM_011533993.1:c.3109C>T
|
XP_011532295.1:p.Gln1037Ter
|
|
XM_011533994.1:c.2818C>T
|
XP_011532296.1:p.Gln940Ter
|
|
XM_005265371.3:c.3112C>T
|
XP_005265428.1:p.Gln1038Ter
|
|
XM_011533993.2:c.3109C>T
|
XP_011532295.1:p.Gln1037Ter
|
|
XM_011533994.2:c.2818C>T
|
XP_011532296.1:p.Gln940Ter
|
|
NM_006514.4:c.3103C>T
MANE Select
|
NP_006505.4:p.Gln1035Ter
|
|