ENST00000300026.4:c.447C>A
(PPIB)
MANE Select
|
ENSP00000300026.4:p.Gly149=
|
|
ENST00000325881.9:c.*2298G>T
(SNX22)
MANE Select
|
ENSP00000323435.4:n.*2298G>T
|
|
ENST00000561048.2:n.3674C>A
(PPIB)
|
|
|
ENST00000680158.1:c.*120C>A
(PPIB)
|
ENSP00000504873.1:n.*120C>A
|
|
ENST00000680343.1:n.401C>A
(PPIB)
|
|
|
ENST00000681397.1:c.447C>A
(PPIB)
|
ENSP00000506584.1:p.Gly149=
|
|
ENST00000681658.1:c.342C>A
(PPIB)
|
ENSP00000505431.1:p.Gly114=
|
|
ENST00000300026.3:c.447C>A
(PPIB)
|
ENSP00000300026.3:p.Gly149=
|
|
ENST00000325881.8:c.*2298G>T
(SNX22)
|
ENSP00000323435.4:n.*2298G>T
|
|
ENST00000557789.5:n.3038G>T
(SNX22)
|
|
|
ENST00000558492.1:n.353C>A
(PPIB)
|
|
|
ENST00000560997.1:n.2693G>T
(SNX22)
|
|
|
NM_000942.4:c.447C>A , LRG_10t1:c.447C>A
(PPIB)
|
NP_000933.1:p.Gly149=
|
|
NM_024798.2:c.*2298G>T
(SNX22)
|
NP_079074.2:n.*2298G>T
|
|
NR_073534.1:n.2986G>T
(SNX22)
|
|
|
XM_017022581.1:c.*2298G>T
(SNX22)
|
XP_016878070.1:n.*2298G>T
|
|
NM_024798.3:c.*2298G>T
(SNX22)
MANE Select
|
NP_079074.2:n.*2298G>T
|
|
NM_000942.5:c.447C>A
(PPIB)
MANE Select
|
NP_000933.1:p.Gly149=
|
|
NR_073534.2:n.2972G>T
(SNX22)
|
|
|