ENST00000300026.4:c.467C>A
(PPIB)
MANE Select
|
ENSP00000300026.4:p.Thr156Lys
|
|
ENST00000325881.9:c.*2278G>T
(SNX22)
MANE Select
|
ENSP00000323435.4:n.*2278G>T
|
|
ENST00000561048.2:n.3694C>A
(PPIB)
|
|
|
ENST00000680158.1:c.*140C>A
(PPIB)
|
ENSP00000504873.1:n.*140C>A
|
|
ENST00000680343.1:n.421C>A
(PPIB)
|
|
|
ENST00000681397.1:c.467C>A
(PPIB)
|
ENSP00000506584.1:p.Thr156Lys
|
|
ENST00000681658.1:c.362C>A
(PPIB)
|
ENSP00000505431.1:p.Thr121Lys
|
|
ENST00000300026.3:c.467C>A
(PPIB)
|
ENSP00000300026.3:p.Thr156Lys
|
|
ENST00000325881.8:c.*2278G>T
(SNX22)
|
ENSP00000323435.4:n.*2278G>T
|
|
ENST00000557789.5:n.3018G>T
(SNX22)
|
|
|
ENST00000558492.1:n.373C>A
(PPIB)
|
|
|
ENST00000560997.1:n.2673G>T
(SNX22)
|
|
|
NM_000942.4:c.467C>A , LRG_10t1:c.467C>A
(PPIB)
|
NP_000933.1:p.Thr156Lys
|
|
NM_024798.2:c.*2278G>T
(SNX22)
|
NP_079074.2:n.*2278G>T
|
|
NR_073534.1:n.2966G>T
(SNX22)
|
|
|
XM_017022581.1:c.*2278G>T
(SNX22)
|
XP_016878070.1:n.*2278G>T
|
|
NM_024798.3:c.*2278G>T
(SNX22)
MANE Select
|
NP_079074.2:n.*2278G>T
|
|
NM_000942.5:c.467C>A
(PPIB)
MANE Select
|
NP_000933.1:p.Thr156Lys
|
|
NR_073534.2:n.2952G>T
(SNX22)
|
|
|