ENST00000599672.6:c.267C>A
MANE Select
|
ENSP00000470560.1:p.His89Gln
|
|
ENST00000261406.7:c.249C>A
|
ENSP00000476966.2:p.His83Gln
|
|
ENST00000539196.2:c.130C>A
|
|
|
ENST00000599672.5:c.267C>A
|
ENSP00000470560.1:p.His89Gln
|
|
ENST00000607161.5:c.270C>A
|
ENSP00000480420.1:p.His90Gln
|
|
ENST00000611981.1:n.278C>A
|
|
|
ENST00000620255.1:n.256C>A
|
|
|
NM_006331.7:c.267C>A
|
NP_006322.4:p.His89Gln
|
|
XM_011520907.1:c.267C>A
|
XP_011519209.1:p.His89Gln
|
|
NM_001320049.1:c.267C>A
|
NP_001306978.1:p.His89Gln
|
|
NR_135131.1:n.410C>A
|
|
|
NM_006331.8:c.267C>A
MANE Select
|
NP_006322.4:p.His89Gln
|
|
NM_001320049.2:c.267C>A
|
NP_001306978.1:p.His89Gln
|
|
NR_135131.2:n.278C>A
|
|
|