|
ENST00000423955.7:c.1239G>T
(KRT86)
MANE Select
|
ENSP00000444533.1:p.Glu413Asp
|
|
|
ENST00000293525.5:c.1239G>T
(KRT86)
|
ENSP00000293525.5:p.Glu413Asp
|
|
|
ENST00000423955.6:c.1239G>T
(KRT86)
|
ENSP00000444533.1:p.Glu413Asp
|
|
|
NM_002284.3:c.1239G>T
(KRT86)
|
NP_002275.1:p.Glu413Asp
|
|
|
XM_005268866.3:c.1470G>T
(KRT86)
|
XP_005268923.1:p.Glu490Asp
|
|
|
XM_011538334.1:c.-212+1939C>A
(KRT81)
|
XP_011536636.1:n.-212+1939C>A
|
|
|
XM_011538336.1:c.1239G>T
(KRT86)
|
XP_011536638.1:p.Glu413Asp
|
|
|
XM_011538337.1:c.1239G>T
(KRT86)
|
XP_011536639.1:p.Glu413Asp
|
|
|
XM_011538338.1:c.1239G>T
(KRT86)
|
XP_011536640.1:p.Glu413Asp
|
|
|
NM_001320198.1:c.1239G>T
(KRT86)
|
NP_001307127.1:p.Glu413Asp
|
|
|
XM_005268866.4:c.1470G>T
(KRT86)
|
XP_005268923.1:p.Glu490Asp
|
|
|
XM_017019296.1:c.1239G>T
(KRT86)
|
XP_016874785.1:p.Glu413Asp
|
|
|
NM_001320198.2:c.1239G>T
(KRT86)
MANE Select
|
NP_001307127.1:p.Glu413Asp
|
|
