ENST00000398015.8:c.806-15913C>T
MANE Select
|
ENSP00000381097.3:n.806-15913C>T
|
|
ENST00000647596.1:c.806-15913C>T
|
ENSP00000497153.1:n.806-15913C>T
|
|
ENST00000398015.7:c.806-15913C>T
|
ENSP00000381097.3:n.806-15913C>T
|
|
ENST00000482618.5:c.*72-15913C>T
|
ENSP00000420338.1:n.*72-15913C>T
|
|
ENST00000488154.5:n.472-15913C>T
|
|
|
ENST00000493838.1:c.-512-15913C>T
|
ENSP00000419574.1:n.-512-15913C>T
|
|
NM_004441.4:c.806-15913C>T
|
NP_004432.1:n.806-15913C>T
|
|
XM_011512540.1:c.788-15913C>T
|
XP_011510842.1:n.788-15913C>T
|
|
XM_011512541.1:c.740-15913C>T
|
XP_011510843.1:n.740-15913C>T
|
|
XM_017005866.2:c.806-15913C>T
|
XP_016861355.1:n.806-15913C>T
|
|
XM_017005867.1:c.788-15913C>T
|
XP_016861356.1:n.788-15913C>T
|
|
XM_024453389.1:c.740-15913C>T
|
XP_024309157.1:n.740-15913C>T
|
|
XM_024453390.1:c.740-15913C>T
|
XP_024309158.1:n.740-15913C>T
|
|
NM_004441.5:c.806-15913C>T
MANE Select
|
NP_004432.1:n.806-15913C>T
|
|