ENST00000273261.8:c.366-11797C>T
MANE Select
|
ENSP00000273261.3:n.366-11797C>T
|
|
ENST00000273261.7:c.366-11797C>T
|
ENSP00000273261.3:n.366-11797C>T
|
|
ENST00000383703.3:c.366-11797C>T
|
ENSP00000373208.3:n.366-11797C>T
|
|
ENST00000475366.5:n.261-11797C>T
|
|
|
ENST00000498287.5:n.319-11797C>T
|
|
|
NM_015541.2:c.366-11797C>T
|
NP_056356.2:n.366-11797C>T
|
|
XM_011533578.1:c.366-11797C>T
|
XP_011531880.1:n.366-11797C>T
|
|
XM_011533579.1:c.-415-11797C>T
|
XP_011531881.1:n.-415-11797C>T
|
|
XM_011533578.2:c.366-11797C>T
|
XP_011531880.1:n.366-11797C>T
|
|
XM_011533579.3:c.-415-11797C>T
|
XP_011531881.1:n.-415-11797C>T
|
|
XM_017006134.2:c.291-11797C>T
|
XP_016861623.1:n.291-11797C>T
|
|
XM_017006136.2:c.-415-11797C>T
|
XP_016861625.1:n.-415-11797C>T
|
|
NM_001377344.1:c.291-11797C>T
|
NP_001364273.1:n.291-11797C>T
|
|
NM_001377345.1:c.-415-11797C>T
|
NP_001364274.1:n.-415-11797C>T
|
|
NM_001377346.1:c.-415-11797C>T
|
NP_001364275.1:n.-415-11797C>T
|
|
NM_015541.3:c.366-11797C>T
MANE Select
|
NP_056356.2:n.366-11797C>T
|
|