ENST00000306875.10:c.1682C>T
MANE Select
|
ENSP00000305459.6:p.Thr561Met
|
|
ENST00000306875.8:c.1682C>T
|
ENSP00000305459.4:p.Thr561Met
|
|
ENST00000562595.5:c.549+4330C>T
|
|
|
ENST00000562949.1:c.352-1817C>T
|
ENSP00000457718.1:n.352-1817C>T
|
|
NM_032382.4:c.1682C>T
|
NP_115758.3:p.Thr561Met
|
|
NM_032382.5:c.1682C>T
MANE Select
|
NP_115758.3:p.Thr561Met
|
|
NM_001379261.1:c.1823C>T
|
NP_001366190.1:p.Thr608Met
|
|
NM_001379262.1:c.1682C>T
|
NP_001366191.1:p.Thr561Met
|
|
NM_001379263.1:c.1721C>T
|
NP_001366192.1:p.Thr574Met
|
|
NM_001379264.1:c.1682C>T
|
NP_001366193.1:p.Thr561Met
|
|
NM_001379265.1:c.1582+1718C>T
|
NP_001366194.1:n.1582+1718C>T
|
|
NM_001379266.1:c.1414-1817C>T
|
NP_001366195.1:n.1414-1817C>T
|
|