ENST00000300026.4:c.432C>G
(PPIB)
MANE Select
|
ENSP00000300026.4:p.Gly144=
|
|
ENST00000325881.9:c.*2313G>C
(SNX22)
MANE Select
|
ENSP00000323435.4:n.*2313G>C
|
|
ENST00000561048.2:n.3659C>G
(PPIB)
|
|
|
ENST00000680158.1:c.*105C>G
(PPIB)
|
ENSP00000504873.1:n.*105C>G
|
|
ENST00000680343.1:n.386C>G
(PPIB)
|
|
|
ENST00000681397.1:c.432C>G
(PPIB)
|
ENSP00000506584.1:p.Gly144=
|
|
ENST00000681658.1:c.327C>G
(PPIB)
|
ENSP00000505431.1:p.Gly109=
|
|
ENST00000300026.3:c.432C>G
(PPIB)
|
ENSP00000300026.3:p.Gly144=
|
|
ENST00000325881.8:c.*2313G>C
(SNX22)
|
ENSP00000323435.4:n.*2313G>C
|
|
ENST00000557789.5:n.3053G>C
(SNX22)
|
|
|
ENST00000558492.1:n.338C>G
(PPIB)
|
|
|
ENST00000560997.1:n.2708G>C
(SNX22)
|
|
|
NM_000942.4:c.432C>G , LRG_10t1:c.432C>G
(PPIB)
|
NP_000933.1:p.Gly144=
|
|
NM_024798.2:c.*2313G>C
(SNX22)
|
NP_079074.2:n.*2313G>C
|
|
NR_073534.1:n.3001G>C
(SNX22)
|
|
|
XM_017022581.1:c.*2313G>C
(SNX22)
|
XP_016878070.1:n.*2313G>C
|
|
NM_024798.3:c.*2313G>C
(SNX22)
MANE Select
|
NP_079074.2:n.*2313G>C
|
|
NM_000942.5:c.432C>G
(PPIB)
MANE Select
|
NP_000933.1:p.Gly144=
|
|
NR_073534.2:n.2987G>C
(SNX22)
|
|
|