ENST00000265963.9:c.347+79A>C
MANE Select
|
ENSP00000265963.4:n.347+79A>C
|
|
ENST00000265963.8:c.347+79A>C
|
ENSP00000265963.4:n.347+79A>C
|
|
ENST00000418116.6:n.546+79A>C
|
|
|
ENST00000453096.6:c.347+79A>C
|
ENSP00000393638.2:n.347+79A>C
|
|
ENST00000534641.5:c.-1-2084A>C
|
ENSP00000435375.1:n.-1-2084A>C
|
|
ENST00000543932.5:n.760+79A>C
|
|
|
NM_001142307.1:c.347+79A>C
|
NP_001135779.1:n.347+79A>C
|
|
NM_005316.3:c.347+79A>C
|
NP_005307.1:n.347+79A>C
|
|
XM_006718208.2:c.347+79A>C
|
XP_006718271.1:n.347+79A>C
|
|
XM_006718208.3:c.347+79A>C
|
XP_006718271.1:n.347+79A>C
|
|
XM_024448457.1:c.347+79A>C
|
XP_024304225.1:n.347+79A>C
|
|
XM_024448458.1:c.347+79A>C
|
XP_024304226.1:n.347+79A>C
|
|
NM_005316.4:c.347+79A>C
MANE Select
|
NP_005307.1:n.347+79A>C
|
|
NM_001142307.2:c.347+79A>C
|
NP_001135779.1:n.347+79A>C
|
|