ENST00000450053.8:c.4061C>T
MANE Select
|
ENSP00000415034.2:p.Thr1354Met
|
|
ENST00000651747.1:c.3959C>T
|
ENSP00000499216.1:p.Thr1320Met
|
|
ENST00000652744.1:n.398C>T
|
|
|
ENST00000416683.5:c.1960-36C>T
|
|
|
ENST00000450053.7:c.4061C>T
|
ENSP00000415034.2:p.Thr1354Met
|
|
NM_015175.2:c.4061C>T , LRG_568t1:c.4061C>T
|
NP_055990.1:p.Thr1354Met
|
|
XM_005264992.2:c.3959C>T
|
XP_005265049.1:p.Thr1320Met
|
|
XM_005264993.2:c.533C>T
|
XP_005265050.1:p.Thr178Met
|
|
XM_006713072.2:c.3980C>T
|
XP_006713135.1:p.Thr1327Met
|
|
XM_011533532.1:c.4040C>T
|
XP_011531834.1:p.Thr1347Met
|
|
XM_011533533.1:c.4061C>T
|
XP_011531835.1:p.Thr1354Met
|
|
XM_011533534.1:c.3692C>T
|
XP_011531836.1:p.Thr1231Met
|
|
XM_011533535.1:c.3521C>T
|
XP_011531837.1:p.Thr1174Met
|
|
XM_011533536.1:c.3407C>T
|
XP_011531838.1:p.Thr1136Met
|
|
XM_011533537.1:c.2969C>T
|
XP_011531839.1:p.Thr990Met
|
|
XR_940397.1:n.4237C>T
|
|
|
XR_940398.1:n.4237C>T
|
|
|
NM_001365116.1:c.3959C>T
|
NP_001352045.1:p.Thr1320Met
|
|
XM_006713072.3:c.3980C>T
|
XP_006713135.1:p.Thr1327Met
|
|
XM_011533533.2:c.4061C>T
|
XP_011531835.1:p.Thr1354Met
|
|
XM_017006010.1:c.4061C>T
|
XP_016861499.1:p.Thr1354Met
|
|
XM_017006011.1:c.4040C>T
|
XP_016861500.1:p.Thr1347Met
|
|
XM_017006012.1:c.3980C>T
|
XP_016861501.1:p.Thr1327Met
|
|
XM_017006013.1:c.4061C>T
|
XP_016861502.1:p.Thr1354Met
|
|
XM_017006014.1:c.3959C>T
|
XP_016861503.1:p.Thr1320Met
|
|
XM_017006015.1:c.3692C>T
|
XP_016861504.1:p.Thr1231Met
|
|
XM_017006016.1:c.3521C>T
|
XP_016861505.1:p.Thr1174Met
|
|
XM_017006017.1:c.533C>T
|
XP_016861506.1:p.Thr178Met
|
|
XR_940397.2:n.4237C>T
|
|
|
NM_001365116.2:c.3959C>T
|
NP_001352045.1:p.Thr1320Met
|
|
NM_015175.3:c.4061C>T
MANE Select
|
NP_055990.1:p.Thr1354Met
|
|