ENST00000515279.6:c.1240+38248A>G
(GSTCD)
MANE Select
|
ENSP00000422354.1:n.1240+38248A>G
|
|
ENST00000360505.9:c.1240+38248A>G
(GSTCD)
|
ENSP00000353695.5:n.1240+38248A>G
|
|
ENST00000394728.4:c.1240+38248A>G
(GSTCD)
|
ENSP00000378216.3:n.1240+38248A>G
|
|
ENST00000394730.7:c.979+38248A>G
(GSTCD)
|
ENSP00000378218.3:n.979+38248A>G
|
|
ENST00000484843.1:n.1491+38248A>G
(GSTCD)
|
|
|
ENST00000510876.1:c.31-67733T>C
(INTS12)
|
ENSP00000422856.1:n.31-67733T>C
|
|
ENST00000515255.5:n.579+38248A>G
(GSTCD)
|
|
|
ENST00000515279.5:c.1240+38248A>G
(GSTCD)
|
ENSP00000422354.1:n.1240+38248A>G
|
|
NM_001031720.3:c.1240+38248A>G
(GSTCD)
|
NP_001026890.2:n.1240+38248A>G
|
|
NM_024751.3:c.979+38248A>G
(GSTCD)
|
NP_079027.2:n.979+38248A>G
|
|
XM_005263222.2:c.1240+38248A>G
(GSTCD)
|
XP_005263279.1:n.1240+38248A>G
|
|
XM_011532248.1:c.1240+38248A>G
(GSTCD)
|
XP_011530550.1:n.1240+38248A>G
|
|
XM_011532249.1:c.1240+38248A>G
(GSTCD)
|
XP_011530551.1:n.1240+38248A>G
|
|
XM_011532250.1:c.1240+38248A>G
(GSTCD)
|
XP_011530552.1:n.1240+38248A>G
|
|
XM_011532251.1:c.1240+38248A>G
(GSTCD)
|
XP_011530553.1:n.1240+38248A>G
|
|
XM_011532252.1:c.1240+38248A>G
(GSTCD)
|
XP_011530554.1:n.1240+38248A>G
|
|
XR_244687.2:n.1191-14446T>C
|
|
|
XR_938771.1:n.1500+38248A>G
(GSTCD)
|
|
|
XM_005263222.4:c.1240+38248A>G
(GSTCD)
|
XP_005263279.1:n.1240+38248A>G
|
|
XM_011532248.3:c.1240+38248A>G
(GSTCD)
|
XP_011530550.1:n.1240+38248A>G
|
|
XM_011532249.3:c.1240+38248A>G
(GSTCD)
|
XP_011530551.1:n.1240+38248A>G
|
|
XM_011532252.3:c.1240+38248A>G
(GSTCD)
|
XP_011530554.1:n.1240+38248A>G
|
|
NM_001370181.1:c.1240+38248A>G
(GSTCD)
MANE Select
|
NP_001357110.1:n.1240+38248A>G
|
|