ENST00000449082.3:c.3191C>T
MANE Select
|
ENSP00000390600.2:p.Thr1064Met
|
|
ENST00000643924.1:c.3188C>T
|
ENSP00000495595.1:p.Thr1063Met
|
|
ENST00000655275.1:c.3215C>T
|
ENSP00000499510.1:p.Thr1072Met
|
|
ENST00000449082.2:c.3191C>T
|
ENSP00000390600.2:p.Thr1064Met
|
|
NM_001293306.2:c.3188C>T
|
NP_001280235.2:p.Thr1063Met
|
|
NM_001293307.2:c.2897C>T
|
NP_001280236.2:p.Thr966Met
|
|
NM_006514.3:c.3191C>T
|
NP_006505.3:p.Thr1064Met
|
|
XM_005265371.2:c.3200C>T
|
XP_005265428.1:p.Thr1067Met
|
|
XM_011533993.1:c.3197C>T
|
XP_011532295.1:p.Thr1066Met
|
|
XM_011533994.1:c.2906C>T
|
XP_011532296.1:p.Thr969Met
|
|
XM_005265371.3:c.3200C>T
|
XP_005265428.1:p.Thr1067Met
|
|
XM_011533993.2:c.3197C>T
|
XP_011532295.1:p.Thr1066Met
|
|
XM_011533994.2:c.2906C>T
|
XP_011532296.1:p.Thr969Met
|
|
NM_006514.4:c.3191C>T
MANE Select
|
NP_006505.4:p.Thr1064Met
|
|